Reported Jul 5, 2023 · Ongoing
Perifix¿ / Epidural anesthesia kit (10 count carton)
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?
- Perifix¿ / Epidural anesthesia kit (10 count carton)
- Lot codes and dates
Model No. 332217332097332220332078
- GTIN
0404696417828304046964177361040469641773610404696417832004046964177200Lot No. 00618507670061855339006185534000618585540061837264
- Amount recalled
- 16,070 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
Kits were assembled with the incorrect Filter Straw.
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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