Reported Nov 9, 2016 · Terminated
Affected Pain Control Tray Component (5% Lidocaine Hydrochloride and 7.5% DExtrose Injection, USP) Injection of…
B. Braun Medical, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: B. Braun Medical, Inc. · 901 Marcon Blvd · Allentown, PA · 18109-9512
Is this the product you have?
- Affected Pain Control Tray Component (5% Lidocaine Hydrochloride and 7.5% DExtrose Injection, USP) Injection of anesthetics to provide regional anesthesia
- Lot codes and dates
- Catalog Number
560399 (Lot # 006141855900614223890061434523006143808400614401880061446168006145097100614592270061464239
- Catalog Number
560511 (Lot # 00614134350061425996006143839300614522720061465310)Catalog # 560605 (006142024000614299620061442280006144951000614604970061471580)Catalog # 560631 (Lot# 0061438803)Catalog # 560632 (0061438818)
- Catalog Number
- Amount recalled
- 1704 units
Where it was sold
Why it was recalled
B. Braun Medical Inc. is voluntarily recalling specific lots of their Custom Spinal Anesthesia Tray which contains a drug component, 5% Lidocaine Hydrochloride and 7.5 % Dextrose Injection, USP that Hospira Inc. has recalled because the drug product does not meet the specification for color throughout shelf life.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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