Brevibloc DOUBLE STRENGTH Premixed Injection recall
Brevibloc DOUBLE STRENGTH Premixed Injection, Esmolol Hydrochloride in Sodium Chloride, 2000mg/100mL (20 mg/mL), 100 mL, Rx only, Manufactured by…
Why was Brevibloc DOUBLE STRENGTH Premixed Injection recalled?
Discoloration: presence of atypical yellow discoloration of the solution .
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 # C989954, Exp 9/17
- Product
- Brevibloc DOUBLE STRENGTH Premixed Injection, Esmolol Hydrochloride in Sodium Chloride, 2000mg/100mL (20 mg/mL), 100 mL, Rx only, Manufactured by…
- Recalling firm
- Baxter Healthcare Corp.
- Quantity
- 11,630 babs
- Distribution
- Nationwide
- Recall date
- May 18, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)