Why it was recalled
Presence of Particulate Matter: identified as glass.
Product description
2% Lidocaine HCl Injection, USP, 100mg/5mL(20mg/mL), Glass ABBOJECT Unit of Use Syringe, packaged as 1 vial and injector per carton, Rx only, Distributed by Hospira Inc., Lake Forest, IL 60045, NDC 0409-4903-11
Lot numbers, UPCs & expiration codes
Lot#: GH6567, Exp. 7/1/2024
Where it was sold
Nationwide in the US and Puerto Rico. The products were not distributed to government accounts or foreign consignees.
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-0102-2024
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- Oct 2, 2023
- FDA report date
- Nov 15, 2023
- Quantity
- 3,200 vials
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Pfizer Inc.
Original FDA data
Every field from FDA enforcement report D-0102-2024, exactly as published.
Show all FDA fields
- City
- New York
- State
- NY
- Status
- Terminated
- Country
- United States
- Event ID
- 93124
- Address
- 235 East 42nd Street
- Code information
- Lot#: GH6567, Exp. 7/1/2024
- Postal code
- 10017-5703
- Report date
- Nov 15, 2023
- Product type
- Drugs
- Recall number
- D-0102-2024
- Classification
- Class I
- Recalling firm
- Pfizer Inc.
- Product quantity
- 3,200 vials
- Termination date
- Feb 14, 2025
- Reason for recall
- Presence of Particulate Matter: identified as glass.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- 2% Lidocaine HCl Injection, USP, 100mg/5mL(20mg/mL), Glass ABBOJECT Unit of Use Syringe, packaged as 1 vial and injector per carton, Rx only, Distributed by Hospira Inc., Lake Forest, IL 60045, NDC 0409-4903-11
- Distribution pattern
- Nationwide in the US and Puerto Rico. The products were not distributed to government accounts or foreign consignees.
- Recall initiation date
- Oct 2, 2023
- Initial firm notification
- Letter
- Center classification date
- Nov 9, 2023