Reported May 8, 2024 · Ongoing
ZPLP Distal Lateral Fibular Plate, Left, 4 Holes, 80 MM, Nonsterile- Indicated for temporary internal fixation and…
Zimmer, 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: Zimmer, Inc. · 1800 W Center St · Warsaw, IN · 46580-2304
Is this the product you have?
- ZPLP Distal Lateral Fibular Plate, Left, 4 Holes, 80 MM, Nonsterile- Indicated for temporary internal fixation and stabilization of
- osteotomies and fractures Item Number00-2357-018-04
- Lot codes and dates
- UDI Number00889024055902
- Lot NumbersLot Number
356 of 356 codes
643629926436299364362994643629956436299664362997643629986436299964363001643630026436300364363004643630056436300664363007643630086436301564363016643630176436301864452231644522326445223364452234644522356445223664452237644522386445223964452240644522416445224264452243644522446445224564452246644522476445224864464613644646146446461664464618644646206446462364464625644646266446462864475451644754526447545364475454644754556447545664482183644821976448228364482341644823806448239364482402
This recall covers 21 products
The agency filed one notice per product. You are reading one of them; the other 20 are below.
8 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention
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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