Reported Jan 23, 2019 · Terminated
Maximum Variable Pitch Compression Screw Caddy, Reference Number 231201003 Product Usage: Intended to carry implants…
Zimmer Biomet, 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 Biomet, Inc. · 56 E Bell Dr · Warsaw, IN · 46582-6989
Is this the product you have?
- Maximum Variable Pitch Compression Screw Caddy, Reference
- Number 231201003 Product UsageIntended to carry implants and instruments during regular inventory distribution and handling and sterilization in the hospitals
- Lot codes and dates
- Lot Numbers
453392453918453919469917475577481064481065486820498695506818512867512868
- Lot Numbers
- Amount recalled
- 971 in total
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
There is a potential for silicone shedding during cleaning and sterilization.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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