Heparin Sodium Injection, USP, 5,000 USP Units/mL, 1mL Multi dose vial Recall 2026
HEPARIN SODIUMIssued October 1, 2026Updated Reviewed by the Recall Watch editorial team
HEPARIN SODIUM Heparin Sodium Injection, USP, 5,000 USP Units/mL, 1mL Multi dose vial x 25 vials per carton, Distributed by: Hepalink USA Inc., Langhome, PA 19047-1885. Carton NDC: NDC 81952-111-06, Vial NDC: 81942 — recalled per FDA on 10/1/2026. Reason: Lack of Assurance of Sterility.
- Agency
- FDA
- Issued
- Oct 1, 2026
- Brand
- HEPARIN SODIUM
- Distribution
- 1 states
- Lots affected
- 2
Steps to take for this recall
Stop using it
Take it out of rotation. Don't consume, wear, or operate.
Verify the match
Compare lot numbers, UPCs, and dates against your product.
Return or dispose
Follow the manufacturer's instructions to refund or safely dispose.
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What's recalled
Heparin Sodium Injection, USP, 5,000 USP Units/mL, 1mL Multi dose vial x 25 vials per carton, Distributed by: Hepalink USA Inc., Langhome, PA 19047-1885. Carton NDC: NDC 81952-111-06, Vial NDC: 81942-111-01

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Why it was recalled
Lack of Assurance of Sterility
Affected products & lot numbers2 lots called out
Affected Lot Numbers
Check your product label — do not use if your lot number appears below.
| Lot Number |
|---|
| Lot# CU03232A |
| Exp 1/31/2028 |
Where was it sold1 state
Nationwide in the USA.
More recalls like this4 related — by brand, contaminant, and category
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Frequently asked questions
Is the HEPARIN SODIUM recall still active?
Yes, this recall is currently active as of October 1, 2026. Do not use or consume the affected product.
What lot numbers are affected?
Affected lot numbers: Lot# CU03232A, Exp 1/31/2028. Check the label on your product.
What should I do if I have the recalled HEPARIN SODIUM?
Do not consume or use this product. Return it to the store for a full refund, or dispose of it safely.