Reported Dec 21, 2022 · Ongoing
DeRoyal TRACECART POSTEROR LUMBAR FUSION TRACECART, REF 53-1961.02
DeRoyal Industries 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: DeRoyal Industries Inc · 200 Debusk Ln · Powell, TN · 37849-4703
Is this the product you have?
- DeRoyal TRACECART POSTEROR LUMBAR FUSION TRACECART, REF 53-1961.02
- Lot codes and dates
- Lot Numbers
56169083 exp 12/01/202356357092 exp 12/01/202356481018 exp 12/01/202356538205 exp 09/01/202356873265 exp 09/01/202356895966 exp 09/01/202356942611 exp 03/01/202457088584 exp 03/01/202457088592 exp 03/01/202457180516 exp 03/01/202457270562 exp 03/01/202457313163 exp 03/01/202457313171 exp 03/01/202457492608 exp 03/01/202457646152 exp 03/01/202457681329 exp 03/01/202457717598 exp 03/01/202457788708 exp 03/01/202457889681 exp 03/01/202457928563 exp 03/01/202457960070 exp 03/01/202458003845 exp 04/01/202458032523 exp 04/01/2024
- Lot Numbers
- Amount recalled
- 336 kits
This recall covers 156 products
The agency filed one notice per product. You are reading one of them; the other 155 are below.
143 more are in the archive.
Where it was sold
Why it was recalled
XXX
This product could cause temporary or reversible health problems — stop using it.
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