Reported Aug 9, 2023 · Ongoing
Equipment and table drapes
Microtek Medical 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: Microtek Medical Inc. · 1 Ecolab Pl · Saint Paul, MN · 55102-2739
Is this the product you have?
14 of 14 products
| Model / number | Barcodes | Product as published |
|---|---|---|
63620RT | (1) - Lot number 220301F, exp 3/3/2027 | |
| — | 00748426129386 | UDI-DI 00748426129386 |
60040S | (2) - Lot number 220305F, exp 3/5/2027 | |
| — | 00748426129348 | UDI-DI 00748426129348 |
60050S | (3) - Lot number 220305F, exp 3/5/2027 | |
| — | 00748426129355 | UDI-DI 00748426129355 |
890017 | (4) - Lot numbers 220110F, exp. 1/10/2027 | |
| — | 220108F, exp 1/8/2027 | |
| — | 220102F, exp 1/2/2027 | |
| — | and 211231F, exp 12/31/2026 | |
| — | 00748426063673 | UDI-DI 00748426063673 |
4951N | and (5) - Lot numbers 220110F, exp 1/10/2027 | |
| — | and 220109F, exp 1/9/2027 | |
| — | 00748426126767 | UDI-DI 00748426126767. |
- Amount recalled
- 9,293 cases/68,070 units for all products
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
Certain lots of the products have a Naphthalene odor.
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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