Why it was recalled
Non-Sterility: Confirmed customer complaint of product contaminated with mold.
Product description
Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA; NDC 0409-7929-09.
Lot numbers, UPCs & expiration codes
Lot #: 05-019-JT*, Exp 05/01/13; lot number * may be followed by 01, 90, or 91.
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-262-2013
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- Jan 25, 2013
- FDA report date
- Apr 24, 2013
- Quantity
- 143,136 flexible containers
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Hospira Inc.
Original FDA data
Every field from FDA enforcement report D-262-2013, exactly as published.
Show all FDA fields
- City
- Lake Forest
- State
- IL
- Status
- Terminated
- Country
- United States
- Event ID
- 64197
- Address
- 275 N Field Dr
- Code information
- Lot #: 05-019-JT*, Exp 05/01/13; lot number * may be followed by 01, 90, or 91.
- Postal code
- 60045-2579
- Report date
- Apr 24, 2013
- Product type
- Drugs
- Recall number
- D-262-2013
- Classification
- Class I
- Recalling firm
- Hospira Inc.
- Product quantity
- 143,136 flexible containers
- Termination date
- Aug 21, 2015
- Reason for recall
- Non-Sterility: Confirmed customer complaint of product contaminated with mold.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA; NDC 0409-7929-09.
- Distribution pattern
- Nationwide
- Recall initiation date
- Jan 25, 2013
- Initial firm notification
- Press Release
- Center classification date
- Apr 17, 2013