Reported Aug 9, 2023 · Ongoing

Equipment and table drapes and Surgical Room Turnover (SRT) Kits

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?

62 of 62 products

Products covered by this recall
Model / numberBarcodesProduct as published
(1) Model ABTSLSAN - Lot numbers 220309D, exp 3/9/2027
and 220302D, exp 3/2/2027
50748426077262UDI-DI 50748426077262
(2) Model ABTSLSN - Lot number 220301D, exp 3/1/2027
50748426077255UDI-DI 50748426077255
ALHS-02(3) - Lot numbers 1392JX0100, exp 9/1/2027
2452JX3000, exp 11/1/2027
3402JX2000, exp 10/1/2027
4382JX0900, exp 9/1/2027
4442JX1100, exp 11/1/2027
and 5422JX0100, 10/1/2027
00748426133512UDI-DI 00748426133512
ALHS-SS-01(4) - Lot number 6382JX1000, exp 9/1/2027
00748426123131UDI-DI 00748426123131
BPGN-02(5) - Lot numbers 2362JX2100, exp 9/1/2027
and 5412JX3200, exp 10/1/2027
00748426080021UDI-DI 00748426080021
HFH-02(6) - Lot number 2362JX1000, exp 9/1/2027
00748426124688UDI-DI 00748426124688
HKHA-02(7) - Lot numbers 1372JX0400, exp 9/1/2027
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.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:42 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.