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Class II: temporary or reversible health riskTerminated

Central Admixture Pharmacy Services Msa 7.84% Msg 8.56% Recall

MSA 7.84% MSG 8.56% (0.92M) Comp. Sol. 1000 ml bag, Rx only, Central Admixture Pharmacy…

Central Admixture Pharmacy Services, Inc. · Allentown, PA

Risk level
Class II
Reported by FDA
May 31, 2023
Recall ID
D-0750-2023
Check your lot numberHow we source this data

Summary

Central Admixture Pharmacy Services recalled Msa 7.84% Msg 8.56% starting Apr 28, 2023. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0750-2023 on May 31, 2023. Reason: Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile. Status: Terminated.

Why it was recalled

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Product description

MSA 7.84% MSG 8.56% (0.92M) Comp. Sol. 1000 ml bag, Rx only, Central Admixture Pharmacy Services, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-8029-1, code 7128580291.

Lot numbers, UPCs & expiration codes

Lot # 37-882955, Exp 04/29/2023; 37-884753, 37-884755, Exp 05/06/2023; 37-887536, 37-887537, Exp 05/17/2023; 37-888532, Exp 05/23/2023; 37-892474, Exp 06/07/2023; 37-896761, Exp 06/23/2023; 37-897261, Exp 06/27/2023

Where it was sold

Nationwide in the USA.

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0750-2023
Classification
Class II
Status
Terminated
Recall initiated
Apr 28, 2023
FDA report date
May 31, 2023
Quantity
653 bags
Recall type
Voluntary: Firm initiated
Recalling firm
Central Admixture Pharmacy Services, Inc.

Original FDA data

Every field from FDA enforcement report D-0750-2023, exactly as published.

Show all FDA fields
City
Allentown
State
PA
Status
Terminated
Country
United States
Event ID
92253
Address
6580 Snowdrift Rd Ste 100
Code information
Lot # 37-882955, Exp 04/29/2023; 37-884753, 37-884755, Exp 05/06/2023; 37-887536, 37-887537, Exp 05/17/2023; 37-888532, Exp 05/23/2023; 37-892474, Exp 06/07/2023; 37-896761, Exp 06/23/2023; 37-897261, Exp 06/27/2023
Postal code
18106-9331
Report date
May 31, 2023
Product type
Drugs
Recall number
D-0750-2023
Classification
Class II
Recalling firm
Central Admixture Pharmacy Services, Inc.
Product quantity
653 bags
Termination date
Jun 22, 2025
Reason for recall
Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Voluntary / mandated
Voluntary: Firm initiated
Product description
MSA 7.84% MSG 8.56% (0.92M) Comp. Sol. 1000 ml bag, Rx only, Central Admixture Pharmacy Services, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-8029-1, code 7128580291.
Distribution pattern
Nationwide in the USA.
Recall initiation date
Apr 28, 2023
Initial firm notification
E-Mail
Center classification date
May 19, 2023

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0750-2023, published May 31, 2023. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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