Why it was recalled
Presence of Particulate Matter: Cardboard
Product description
Vancomycin Hydrochloride for Injection, USP, 10 g, 100 mL vial, Rx only, Hospira, Lake Forest, IL, NDC 0409-6510-01
Lot numbers, UPCs & expiration codes
Lot #:565003A, Exp.01 Aug 2017
Where it was sold
Nationwide
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-1033-2016
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- May 6, 2016
- FDA report date
- Jun 22, 2016
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Hospira Inc.
Original FDA data
Every field from FDA enforcement report D-1033-2016, exactly as published.
Show all FDA fields
- City
- Lake Forest
- State
- IL
- Status
- Terminated
- Country
- United States
- Event ID
- 73992
- Address
- 275 N Field Dr
- Code information
- Lot #:565003A, Exp.01 Aug 2017
- Postal code
- 60045-2579
- Report date
- Jun 22, 2016
- Product type
- Drugs
- Recall number
- D-1033-2016
- Classification
- Class II
- Recalling firm
- Hospira Inc.
- Termination date
- Sep 24, 2018
- Reason for recall
- Presence of Particulate Matter: Cardboard
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Vancomycin Hydrochloride for Injection, USP, 10 g, 100 mL vial, Rx only, Hospira, Lake Forest, IL, NDC 0409-6510-01
- Distribution pattern
- Nationwide
- Recall initiation date
- May 6, 2016
- Initial firm notification
- Letter
- Center classification date
- Jun 15, 2016