Reported Jul 12, 2023 · Ongoing
Custom medical procedure packs labeled as: a) STURDI STRAINER TRAY STANDARD, REF '89-5014
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?
- Custom
- medical procedure packs labeled asa) STURDI STRAINER TRAY STANDARD, REF '89-5014
- Lot codes and dates
a) REF '89-5014GTIN 50749756217908 (cs)00749756217903 (unit)
- Lot Numbers58770294
- Amount recalled
- 40 units
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
- Nationwide
Why it was recalled
The outer package seal could be open, or compromised which affects the sterility of the procedure pack inside.
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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