Cefoxitin for Injection and Dextrose Injection recall: Particulate Matter
Cefoxitin for Injection and Dextrose Injection, 1 g in Duplex, 50 mL Container, Catalog No. 3123-11, For IV Use Only, Single Use, Sterile, Rx Only, B…
Why was Cefoxitin for Injection and Dextrose Injection recalled?
Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.
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# H3E507, Exp 11/14
- Product
- Cefoxitin for Injection and Dextrose Injection, 1 g in Duplex, 50 mL Container, Catalog No. 3123-11, For IV Use Only, Single Use, Sterile, Rx Only, B…
- Recalling firm
- B. Braun Medical Inc
- Quantity
- 22,584 units
- Distribution
- Nationwide, Puerto Rico and Spain
- Recall date
- May 7, 2014
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)