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Class II: temporary or reversible health riskTerminated

Central Admixture Pharmacy Services oxyTOCIN 30 units added to 0 Recall

oxyTOCIN 30 units added to 0

Central Admixture Pharmacy Services, Inc. · Phoenix, AZ

Risk level
Class II
Reported by FDA
Sep 6, 2023
Recall ID
D-1133-2023
Check your lot numberHow we source this data

Summary

Central Admixture Pharmacy Services recalled oxyTOCIN 30 units added to 0 starting Aug 17, 2023. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1133-2023 on Sep 6, 2023. Reason: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles. Status: Terminated.

Why it was recalled

Lack of Assurance of Sterility:Lack of validation data for sanitization cycles

Product description

oxyTOCIN 30 units added to 0.9% sodium chloride 500 mL, IV Bag, Rx only, CAPS, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-6044-1

Lot numbers, UPCs & expiration codes

Lot# 36-260031, 36-260027, Exp 10/3/2023; 36-262533,36-262532, 36-262531, 36-262530, 36-262529, 36-262528, 36-262527, Exp 10/9/2023. ;

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-1133-2023
Classification
Class II
Status
Terminated
Recall initiated
Aug 17, 2023
FDA report date
Sep 6, 2023
Quantity
2643 bags
Recall type
Voluntary: Firm initiated
Recalling firm
Central Admixture Pharmacy Services, Inc.

Original FDA data

Every field from FDA enforcement report D-1133-2023, exactly as published.

Show all FDA fields
City
Phoenix
State
AZ
Status
Terminated
Country
United States
Event ID
92898
Address
2200 S 43rd Ave
Code information
Lot# 36-260031, 36-260027, Exp 10/3/2023; 36-262533,36-262532, 36-262531, 36-262530, 36-262529, 36-262528, 36-262527, Exp 10/9/2023. ;
Postal code
85043-3909
Report date
Sep 6, 2023
Product type
Drugs
Recall number
D-1133-2023
Classification
Class II
Recalling firm
Central Admixture Pharmacy Services, Inc.
Product quantity
2643 bags
Termination date
Mar 27, 2025
Reason for recall
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Voluntary / mandated
Voluntary: Firm initiated
Product description
oxyTOCIN 30 units added to 0.9% sodium chloride 500 mL, IV Bag, Rx only, CAPS, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-6044-1
Distribution pattern
Nationwide in the USA
Recall initiation date
Aug 17, 2023
Initial firm notification
Letter
Center classification date
Aug 28, 2023

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1133-2023, published Sep 6, 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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