D-0080-2018 Class II Terminated
FDA drug recall D-0080-2018 was initiated by PharMEDium Services, LLC. on October 13, 2017 and is designated Class II. Reason for recall: Superpotent drug: out of specification result for potency The recall status is terminated (terminated January 24, 2020). Affected quantity: 499 syringes.
Recall Details
- Product Type
- Drugs
- Report Date
- November 22, 2017
- Initiation Date
- October 13, 2017
- Termination Date
- January 24, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 499 syringes
Product Description
Hydromorphone HCl 0.5 mg per mL in 0.9% Sodium Chloride Injection 1 mL, packaged in syringes, Rx Only , PharMEDium Services, LLC. 913 N. Davis Ave Cleveland, MS 38732, NDC 61553-352-40
Reason for Recall
Superpotent drug: out of specification result for potency
Distribution Pattern
CA, IL
Code Information
Lot#: 172820134M, Exp 01/18