Reported Dec 9, 2020 · Terminated
PROCEED Surgical Mesh Hernia Mesh Oval, 15 cm x 20 cm
Ethicon, 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: Ethicon, Inc. · Us Highway 22 West · Somerville, NJ · 08876
Is this the product you have?
- PROCEED Surgical Mesh Hernia Mesh Oval, 15 cm x 20 cm
- Lot codes and dates
- Product Code - PCDG1 Product Lot - PHG118 GTIN
- Code - 10705031047716 Expiration Date07/31/2021
- Amount recalled
- 295 units distributed. Only 15 units are being recalled.
Why it was recalled
The firm is recalling the PROCEED Surgical Mesh device, because it is a sterile device, and a customer found a hair inside of the primary packaging of a single unit.
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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