Equipment and table drapes and Surgical Room Turnover — Class II medical device recall Z-2251-2023
Ongoing recall by Microtek Medical Inc., reported 2023-08-09, distributed nationwide. Certain lots of the products have a Naphthalene odor.
| Recall number | Z-2251-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Microtek Medical Inc., Saint Paul, MN, United States |
| Recall initiated | 2023-06-23 |
| Classified | 2023-07-28 |
| Reported by FDA | 2023-08-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| UPC / GTIN / UDI-DI | 00748426068258, 00748426077809, 00748426078417, 00748426078813, 00748426078837, 00748426080021, 00748426082803, 00748426109326, 00748426115228, 00748426123131, 00748426124688, 00748426125753, 00748426128723, 00748426132034, 00748426133512, 50748426077255, 50748426077262 |
| Lot numbers | 1362JX0300, 1372JX0200, 1372JX0400, 1392JX0100, 1442JX0600, 2013JX3400, 220301D, 220302D, 220309D, 2332JX0900, 2342JX0100, 2362JX1000, 2362JX2100, 2412JX2300, 2412JX3300, 2422JX1900, 2422JX2200, 2432JX1700, 2452JX3000, 3282JX2500, 3362JX1200, 3382JX2100, 3392JX0100, 3402JX1300, 3402JX2000, 3412JX0700, 4023JX3100, 4382JX0900, 4442JX1100, 5312JX0100, 5322JX1100, 5332JX2100, 5372JX0700, 5412JX3200, 5422JX0100, 6282JX2600, 6372JX1200, 6372JX1300, 6382JX1000, 6422JX0700 and 4 more |
| Model numbers | 10/CASE, 12/CASE, 15/CASE, 9/CASE, ALHS-02, ALHS-SS-01, BPGN-02, HFH-02, HKHA-02, HMC-06, JFKSC-01, LH-LD-05, NEGM-CV-01D, PMMC-02D, PMMC-SP-01D, R-01D, UCLA-LD-03, VAIC-03, VAIC-CP-02, VB-OSC-01 |
| Expiration dates | 2027-03-01, 2027-03-02, 2027-03-09, 2027-07-01, 2027-08-01, 2027-08-12, 2027-09-01, 2027-09-05, 2027-09-16, 2027-10-01, 2027-11-01, 2028-01-03 |
Product
Equipment and table drapes and Surgical Room Turnover (SRT) Kits: (1) Ecolab Absorbent Table Cover W/Transfer Sheet & Armboard Covers, Model #ABTSLSAN, 20/case, non-sterile; (2) Microtek/Ecolab/CleanOp Absorbent Table Cover w/Transfer Sheet, Model ABTSLSN, 25/case, non-sterile; Surgical Room Turnover (SRT) Kits: (3) Ecolab Genesys CleanOp Infection Control System, Model ALHS-02, 12/case, non-sterile; (4) Ecolab Genesys CleanOp Infection Control System, Model ALHS-SS-01, 12/case, non-sterile; (5) Ecolab CleanOp Infection Control System, Model BPGN-02, 10/case, non-sterile; (6) Ecolab Genesys CleanOp Infection Control System, Model HFH-02, 12/case, non-sterile; (7) Ecolab Genesys CleanOp Infection Control System, Model HKHA-02, 15/case, non-sterile; (8) Ecolab CleanOp Infection Control System, Model JFKSC-01, 15/case, non-sterile; (9) Ecolab Genesys CleanOp Infection Control System, Model LH-LD-05, 12/case, non-sterile; (10) Ecolab CleanOp Infection Control System, Model NEGM-CV-01D, 9/case, non-sterile; (11) Ecolab Genesys CleanOp Infection Control System, Model PMMC-02D, 12/case, non-sterile; (12) Ecolab Genesys CleanOp Infection Control System, Model PMMC-SP-01D, 12/case, non-sterile; (13) Ecolab Genesys CleanOp Infection Control System, Model SHMC-06, 15/case, non-sterile; (14) Ecolab CleanOp Infection Control System, Model SR-01D, 12/case, non-sterile; (15) Ecolab CleanOp Infection Control System, Model SVB-OSC-01, 12/case, non-sterile; (16) Ecolab CleanOp Infection Control System, Model UCLA-LD-03, 12/case, non-sterile; (17) Ecolab CleanOp Infection Control System, Model VAIC-03, 12/case, non-sterile; and (18) Ecolab Genesys CleanOp Infection Control System, Model VAIC-CP-02, 15/case, non-sterile.
Reason for recall
Certain lots of the products have a Naphthalene odor.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2251-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.