Brevibloc DOUBLE STRENGTH Premixed Injection, Esmolol Hydrochloride in Sodium Chloride, 2000mg/100mL (20 mg/mL), 100 mL, Rx only, Manufactured by Baxter Healthcare Corporation, Deerfield, Il 60015, NDC 10019-075-87
Reported: May 18, 2016 Initiated: April 12, 2016 #D-0852-2016
Product Description
Brevibloc DOUBLE STRENGTH Premixed Injection, Esmolol Hydrochloride in Sodium Chloride, 2000mg/100mL (20 mg/mL), 100 mL, Rx only, Manufactured by Baxter Healthcare Corporation, Deerfield, Il 60015, NDC 10019-075-87
Reason for Recall
Discoloration: presence of atypical yellow discoloration of the solution .
Details
- Recalling Firm
- Baxter Healthcare Corp.
- Units Affected
- 11,630 babs
- Distribution
- Nationwide
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
Brevibloc DOUBLE STRENGTH Premixed Injection, Esmolol Hydrochloride in Sodium Chloride, 2000mg/100mL (20 mg/mL), 100 mL, Rx only, Manufactured by Baxter Healthcare Corporation, Deerfield, Il 60015, NDC 10019-075-87. Recalled by Baxter Healthcare Corp.. Units affected: 11,630 babs.
Why was this product recalled? ▼
Discoloration: presence of atypical yellow discoloration of the solution .
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on May 18, 2016. Severity: Moderate. Recall number: D-0852-2016.
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