Magnesium Sulfate Injection recall
Magnesium Sulfate Injection, USP, 50%, 20mL, Single dose Fliptop Vial, For IV or IM use, Rx only, Manufactured by Hospira, Inc. 4285 Wesleyan Blvd…
Why was Magnesium Sulfate Injection recalled?
Failed pH Specifications: 12 month stability testing
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: 39-569-DK, Exp 3/1/2016
- Product
- Magnesium Sulfate Injection, USP, 50%, 20mL, Single dose Fliptop Vial, For IV or IM use, Rx only, Manufactured by Hospira, Inc. 4285 Wesleyan Blvd…
- Recalling firm
- Hospira Inc.
- Quantity
- 106,900 vials
- Distribution
- U.S. Nationwide, Kuwait, Bahrain and Israel.
- Recall date
- July 15, 2015
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)