ADSOL RED CELL PRESERVATION- anticoagulant citrate phosphate dextrose (cpd) and adsol preservation kit 
Fenwal, Inc.

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CPD/ADSOL- anticoagulant citrate phosphate dextrose (cpd) and adsol preservation

BLOOD-PACK UNIT

Blood-Pack Unit with an Integral Bioflex RC Leukocyte Reduction Filter Using CPD/Adsol Red Cell Preservation Solution for Whole Blood Collection and Filtration of Red Blood Cells

Rx only


Contains Y-Sampling Site for the collection of unanticoagulated whole blood samples for laboratory testing.

Integral filter unit intended for leukocyte reduction of AS-1 red blood cells:

At ambient temperature up to 8 hours after blood collection.
At refrigerated temperature up to 3 days after blood collection if AS-1 red blood cells are prepared within 3 days after whole blood collection.
The leukocyte reduced red blood cells may then be stored for the maximum allowable dating period.


Instructions for Use
Collection Procedure:
Use aseptic technique.


Notes:



Precautions:

1. Identify Blood-Pack Unit using appropriate donor identification system.

2. Adjust donor scale to desired collection weight and position primary container on the donor scale as far as possible below donor arm.

3. Clamp donor tubing between needle and primary container. (This step may be performed prior to step 1 or 2.)

4. Following blood center procedures, apply pressure to donor’s arm and disinfect site of venipuncture.

5. Remove needle cover per instructions below:

a) Holding the hub and cover near the tamper-evident seal, twist cover and hub in opposite directions to break seal.

b) Remove needle cover, being careful not to drag the cover across the needle point.

6. Following blood center procedures, perform venipuncture, appropriately secure donor needle and/or tubing and release clamp on donor tubing.

7. When good blood flow is established, stabilize the front of the needle guard to arm with tape (see Figure 1).

8. Mix blood and anticoagulant in the primary container immediately, at several intervals during collection, and immediately after collection.

9. Collect the appropriate volume based on Blood-Pack Unit used.

Note: The volume of anticoagulant is sufficient for the blood collection indicated on Blood-Pack Unit ±10%.

10. Release the pressure on the donor’s arm as appropriate.

Precaution: Do not proceed with the remaining steps until the entire whole blood unit is collected.

11. To avoid possible contamination of the whole blood unit, before filling whole blood sample tubes, hermetically seal the donor tubing near the Y-Sampling Site on the side leading to the primary container using a metal clip or appropriate alternate method.

Precaution: Complete steps 12 – 21 within approximately 4 minutes after sealing the donor tubing to avoid possible clot formation in the tubing.

12. To collect samples, insert the access device by pushing firmly into the Y-Sampling Site until the membrane seal is penetrated (see Figure 2).

Note: If the access device is assembled such that the outer barrel is screwed onto the Luer, make sure to rotate clockwise upon insertion to avoid barrel detaching from Luer.

13. Open the cap on the access device (if applicable).

14. Directly align the vacuum sample tube with the internal needle in the access device. Insert vacuum sample tube into device until the stopper is punctured.

15. Allow vacuum sample tube to fill with blood, then remove from the access device.

16. Repeat steps 14 and 15 until the desired number of vacuum sample tubes have been filled.

Notes: 

 

Precaution: When replacing the access device, be careful to avoid contact with any blood droplets on the Luer or Sampling Site. Discard used access device appropriately.

17. Release pressure on donor's arm.

18. If appropriate, apply clamp to donor tubing between needle and Y-Sampling Site.

19. Withdrawal of Needle (see Figure 3).

Precaution: The needle guard must be held stationary while the needle is withdrawn into it.

a) Place folded sterile gauze over puncture site and hold in place with fingertip without exerting pressure.

b) Hold sides of needle guard near the front, between the index finger and thumb. Pull the hub back smoothly until the needle is completely enclosed and securely locked into the needle guard.

c) Confirm the needle is completely enclosed and securely locked into the needle guard.

20. Remove and discard the Y-Sampling Site and needle guard into an appropriate biohazardous waste container following established procedures. If donor tubing is also to be discarded, hermetically seal donor tubing directly above the primary container and remove.

Note: Step 21 may be performed prior to step 20 if desired.

21. If the donor tubing is not hermetically sealed directly above the primary container, then strip the blood from the remaining donor tubing into the primary container and mix. If desired, allow tubing to refill.



Component Preparation:

Notes:

     a) Within 8 hours of blood collection if whole blood is held at ambient temperature.

     b) Within 3 days of blood collection if whole blood is refrigerated.

22. At the appropriate time, prepare the Blood-Pack Unit with Integral Filter for centrifugation.

23. Thoroughly mix the primary container end over end.

24. Load the Blood-Pack Unit into a centrifuge cup per the instructions on page 3 or 4.
Page 3 describes Option A, the method of centrifuge cup loading when using standard oval centrifuge cups.
Page 4 describes Option B, the method of centrifuge cup loading when using large oval centrifuge cups. this method differs from Option A in steps 7 - 9 only and shows the use of a blood bag insert to help fill extra space inside the cup.

Notes:

25. After loading the Blood-Pack unit into the centrifuge cup, perform centrifugation according to center procedures.

26. Following centrifugation, remove containers from the centrifuge cup taking care not to disturb the red blood cell / plasma interface.

27. Place the primary container in a plasma extractor and apply pressure. Clamp off tubing above the filter to prevent plasma flow into the filter during plasma transfer. If applicable, clamp off tubing below the Y-Junction leading to the secondary Transfer-Pack container not to be filled with plasma. Open the cannula on the top of the primary container to transfer plasma into the empty Transfer-Pack container.

28. When the desired amount of plasma has been removed, clamp the tubing between the plasma container and the Y- connector closest to the plasma container and release pressure on the primary container. Seal and remove satellite container(s).

29. Suspend the Adsol red cell preservation solution container, ensuring that the primary container remains below the level of the filter during prime. Open the cannula on the Adsol solution container and remove the clamp between the primary container and the filter. Allow the Adsol to drain through the filter into the primary container. Clamp the tubing between the filter and the primary container after prime is complete.

30. Mix the Adsol red cell preservation solution and red cells thoroughly.

Note: If the Adsol red cell preservation solution is not added to the red cells, ensure appropriate labeling of the red cell container. Also ensure that tubing with unique segment numbers are attached as the primary container does not include tubing with segment numbers. Manufacture of CPD Red Cells for transfusion must include proper labeling of the container as well as attached tubing with unique segment numbers. A CPD red cell without Adsol red cell preservation solution may be stored between 1 and 6ºC up to 21 days after collection. The attached Bioflex RC filter should not be
used to leukoreduce a CPD red cell without Adsol red cell preservation solution.



Filtration Procedure:

Precaution: Red blood cell products collected from certain donors may have extended filtration times and the potential for ineffective filtration and leukoreduction.

31. Mix unfiltered AS-1 red blood cells thoroughly. Invert the unfiltered AS-1 red blood cells and hang the filter set such that the filter remains vertical. Filtration may be performed from 165 cm up to full length. To achieve maximum flow rate, allow the set to hang to full length. The storage container must remain below the level of the filter during filtration.

32. Filtration must be initiated up to 8 hours after collection at ambient condition, or up to 3 days at refrigerated temperature.

33. Inspect all tubing to ensure it hangs freely without kinks.

34. Remove the clamp above the filter to start filtration.

Note: Manual or mechanical pressure should not be used to increase the flow rate through the filter. Tubing below the filter should not be stripped at any time during the filtration process.


Note:
If filtration of red cells is initiated at ambient temperature, the filtration process can be completed at either ambient or refrigerated temperature prior to storing the red cells between 1 and 6°C. However, for optimal filtration time, it is recommended to complete the filtration at ambient temperature.

fig01
fig02
fig03
35. When filtration is complete, air can be observed in the inlet side of the filter. Hermetically seal and detach the tubing below the filter.

36. Make segments from the post filter tubing and leave segments attached to the filtered red cell storage container. (QC samples may be prepared by thoroughly mixing the filtered red cells and stripping this tubing prior to sealing the segments.)

37. Store the AS-1 red blood cells, leukocytes reduced between 1 and 6°C.

38. Infuse the red cells within 42 days of collection.

39. Percent red blood cell recovery should be determined per FDA Guidance entitled "Guidance for Industry – Pre-Storage Leukocyte Reduction of Whole Blood and Blood Components Intended for Transfusion", current issue.

Warning: Failure to achieve closed system processing conditions negates the extended storage claim and the red blood cell product must be transfused within 24 hours.
fig04

Clinical Studies:

Data table below represents a summary of data generated under study protocol LERF-003-CMD. These data summarize Fenwal Bioflex RC filter performance under defined conditions of product usage.
tab01
opa1
opa2
opb1
opb2
Store at Controlled Room Temperature. Protect from freezing. Avoid excessive heat.

Definition of "Controlled Room Temperature":

"A temperature maintained thermostatically that encompasses the usual and customary working environment of 20° to 25°C (68° to 77°F); that results in a mean kinetic temperature calculated to be not more than 25°C; and that allows for excursions between 15°C and 30°C (59° and 86°F) that are experienced in pharmacies, hospitals, and warehouses. Provided the mean kinetic temperature remains in the allowed range, transient spikes up to 40°C are permitted as long as they do not exceed 24 hours ... The mean kinetic temperature is a calculated value that may be used as an isothermal storage temperature that simulates the non isothermal effects of storage temperature variations."

Reference: United States Pharmacopeia, General Notices. United States Pharmacopeial Convention, Inc. 12601 Twinbrook
Parkway, Rockville, MD.

mfg
Fenwal, Inc.
Lake Zurich, IL 60047 USA

1-800-933-6925
© 2019 Fenwal, Inc. All rights reserved.

Fenwal, Blood-Pack, Transfer-Pack, Adsol, and Bioflex RC are trademarks of Fenwal, Inc.
Sorvall us a trademark of Thermo Fisher Scientific LLC.
Beckman is a trademark of Beckman Coulter, Inc.

07-19-13-426 REV: A 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Anticoagulant Citrate Phosphate Dextrose Solution, USP (CPD) BLOOD-PACK Unit; TRANSFER-PACK Container with ADSOL Red Cell Preservation Solution; Integral FENWAL BIOFLEX RC Red Cell Leukocyte Reduction Filter

Double For The Collection and Processing of 500 mL Blood
Y-Sampling Site, 16 ga. Ultra Thin Wall Needle

Rx only

Each unit consists of a PL146 Plastic primary container with 70 mL of CPD solution containing 1.84 g Sodium Citrate (dihydrate) USP, 1.78 g Dextrose (monohydrate) USP, 209 mg Citric Acid (anhydrous) USP, 155 mg Monobasic Sodium Phosphate (monohydrate) USP, pH may have been adjusted with sodium hydroxide; one empty 400 mL PL2209 Plastic TRANSFER-PACK container; one integral FENWAL BIOFLEX RC Red Cell Leukocyte reduction filter and one 450 mL PL2209 Plastic TRANSFER-PACK container with 110 mL of ADSOL Red Cell Preservation Solution containing 2.42 g Dextrose (monohydrate) USP, 990 mg Sodium Chloride USP, 825 mg Mannitol USP, 30 mg Adenine USP for the storage of AS-1 red blood cells, leukocytes reduced.


Sterile, non-pyrogenic fluid path.

See instructions for use.


Store at Controlled Room Temperature (refer to direction insert).


        I)                   Units are not removed from foil pouch, or

        II)                Unused units removed from foil pouch are returned to the foil pouch within 12 hours. Units may be removed from the pouch and returned only once.


FENWAL, BLOOD-PACK, ADSOL, BIOFLEX RC, and TRANSFER-PACK are trademarks of Fenwal, Inc.


Fenwal, Inc.

Lake Zurich, IL 60047 USA

Made in USA


07-28-10-990 REV: A

label

ADSOL RED CELL PRESERVATION 
anticoagulant citrate phosphate dextrose (cpd) and adsol preservation kit kit
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0942-6504
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0942-6504-021 in 1 KIT; Type 1: Convenience Kit of Co-Package
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 BAG 70 mL
Part 21 BAG 110 mL
Part 1 of 2
CPD 
citrate phosphate dextrose solution
Product Information
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID1.84 g  in 70 mL
DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE1.78 g  in 70 mL
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID209 mg  in 70 mL
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN) (PHOSPHATE ION - UNII:NK08V8K8HR) SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE155 mg  in 70 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
170 mL in 1 BAG; Type 1: Convenience Kit of Co-Package
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDABN811104
Part 2 of 2
ADSOL RED CELL PRESERVATION 
adsol red cell preservation solution
Product Information
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE2.42 g  in 110 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE990 mg  in 110 mL
MANNITOL (UNII: 3OWL53L36A) (MANNITOL - UNII:3OWL53L36A) MANNITOL825 mg  in 110 mL
ADENINE (UNII: JAC85A2161) (ADENINE - UNII:JAC85A2161) ADENINE30 mg  in 110 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1110 mL in 1 BAG; Type 1: Convenience Kit of Co-Package
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDABN81110402/28/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDABN81110402/28/2017
Labeler - Fenwal, Inc. (794519020)
Establishment
NameAddressID/FEIBusiness Operations
Fenwal International, Inc.091164590MANUFACTURE(0942-6504)

Revised: 10/2020
Document Id: 8f0e68b0-7eba-4723-8c67-694679d2e621
Set id: 70e80180-f323-4c74-ac2f-f8a53fde91bc
Version: 4
Effective Time: 20201012
 
Fenwal, Inc.