HEPARIN Sodium Inj., USP, 5,000 USP Heparin Units per 5 mL Total Volume in a syringe, NOT FOR LOCK FLUSH, 1,000 USP Heparin Units per mL, Rx only, PharMEDium, Product code 2K1925.
Reported: October 19, 2016 Initiated: July 17, 2015 #D-0048-2017
Product Description
HEPARIN Sodium Inj., USP, 5,000 USP Heparin Units per 5 mL Total Volume in a syringe, NOT FOR LOCK FLUSH, 1,000 USP Heparin Units per mL, Rx only, PharMEDium, Product code 2K1925.
Reason for Recall
Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
Details
- Recalling Firm
- Pharmedium Services, LLC
- Units Affected
- 240 syringes
- Distribution
- Nationwide
- Location
- Lake Forest, IL
Frequently Asked Questions
What product was recalled? ▼
HEPARIN Sodium Inj., USP, 5,000 USP Heparin Units per 5 mL Total Volume in a syringe, NOT FOR LOCK FLUSH, 1,000 USP Heparin Units per mL, Rx only, PharMEDium, Product code 2K1925.. Recalled by Pharmedium Services, LLC. Units affected: 240 syringes.
Why was this product recalled? ▼
Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on October 19, 2016. Severity: Moderate. Recall number: D-0048-2017.
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