TMJ Arthroscopy Drape — Class II medical device recall Z-1071-2022
Terminated recall by Microtek Medical Inc., reported 2022-05-18, distributed nationwide. Latex content in product was labeled incorrectly as latex free.
| Recall number | Z-1071-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Microtek Medical Inc., Saint Paul, MN, United States |
| Recall initiated | 2022-04-08 |
| Classified | 2022-05-12 |
| Reported by FDA | 2022-05-18 |
| Terminated | 2024-06-05 |
| Distributed | Nationwide (US) |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 50748426008556 |
| Lot numbers | D181232, D181982, D202232, D210742, D211372, D212562, D213122, D213402 |
| Expiration dates | 2022-05-01, 2022-07-01, 2024-08-01, 2025-03-01, 2025-05-01, 2025-09-01, 2025-11-01, 2025-12-01 |
Product
TMJ Arthroscopy Drape, 85''x 96''
Reason for recall
Latex content in product was labeled incorrectly as latex free.
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-1071-2022. 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.