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Class II: temporary or reversible health riskTerminated

Central Admixture Pharmacy Services HYDROmorphone added to 0 Recall

HYDROmorphone added to 0

Central Admixture Pharmacy Services Inc · San Diego, CA

Risk level
Class II
Reported by FDA
Aug 9, 2023
Recall ID
D-1052-2023
Check your lot numberHow we source this data

Summary

Central Admixture Pharmacy Services recalled HYDROmorphone added to 0 starting Jul 17, 2023. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1052-2023 on Aug 9, 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

HYDROmorphone added to 0.9% sodium chloride, 10 mg/50 mL, (0.2 mg/mL), 100 mL bag, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-2010-3

Lot numbers, UPCs & expiration codes

Lot: 17-270599, 17-270600, Exp. 7/17/2023; 17-270785, Exp. 7/19/2023; 17-270969, Exp. 7/23/2023; 17-271116, 17-271135, Exp. 7/25/2023; 17-271242, Exp. 7/26/2023; 17-271502, Exp. 7/31/2023; 17-271561, 17-271589, Exp. 8/1/2023; 17-271672, Exp. 8/2/2023; 17-271837, Exp. 8/6/2023; 17-272291, Exp. 8/14/2023; 17-272363, 17-272364, Exp. 8/15/2023; 17-272453, Exp. 8/16/2023; 17-272607, Exp. 8/20/2023; 17-272706, Exp. 8/21/2023; 17-273148, Exp. 8/29/2023; 17-273421, Exp. 9/3/2023; 17-273698, 17-273700, Exp. 9/6/2023; 17-273966, Exp. 9/11/2023.

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-1052-2023
Classification
Class II
Status
Terminated
Recall initiated
Jul 17, 2023
FDA report date
Aug 9, 2023
Quantity
3824 bags
Recall type
Voluntary: Firm initiated
Recalling firm
Central Admixture Pharmacy Services Inc

Original FDA data

Every field from FDA enforcement report D-1052-2023, exactly as published.

Show all FDA fields
City
San Diego
State
CA
Status
Terminated
Country
United States
Event ID
92752
Address
7935 Dunbrook Rd Ste C
Code information
Lot: 17-270599, 17-270600, Exp. 7/17/2023; 17-270785, Exp. 7/19/2023; 17-270969, Exp. 7/23/2023; 17-271116, 17-271135, Exp. 7/25/2023; 17-271242, Exp. 7/26/2023; 17-271502, Exp. 7/31/2023; 17-271561, 17-271589, Exp. 8/1/2023; 17-271672, Exp. 8/2/2023; 17-271837, Exp. 8/6/2023; 17-272291, Exp. 8/14/2023; 17-272363, 17-272364, Exp. 8/15/2023; 17-272453, Exp. 8/16/2023; 17-272607, Exp. 8/20/2023; 17-272706, Exp. 8/21/2023; 17-273148, Exp. 8/29/2023; 17-273421, Exp. 9/3/2023; 17-273698, 17-273700, Exp. 9/6/2023; 17-273966, Exp. 9/11/2023.
Postal code
92126-6322
Report date
Aug 9, 2023
Product type
Drugs
Recall number
D-1052-2023
Classification
Class II
Recalling firm
Central Admixture Pharmacy Services Inc
Product quantity
3824 bags
Termination date
Mar 21, 2025
Reason for recall
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Voluntary / mandated
Voluntary: Firm initiated
Product description
HYDROmorphone added to 0.9% sodium chloride, 10 mg/50 mL, (0.2 mg/mL), 100 mL bag, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-2010-3
Distribution pattern
Nationwide in the USA
Recall initiation date
Jul 17, 2023
Initial firm notification
Letter
Center classification date
Aug 3, 2023

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1052-2023, published Aug 9, 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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