FDA Device recall Z-1071-2022
TMJ Arthroscopy Drape, 85''x 96''
- FDA Device
- Class II
- terminated
- Published 2022-05-18
On 2022-05-18 the FDA classified a Class II recall of TMJ Arthroscopy Drape, 85''x 96'' by Microtek Medical, citing latex content in product was labeled incorrectly as latex free.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1071-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-04-08 |
| Published | 2022-05-18 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Microtek Medical |
| Distribution | US |
Product
TMJ Arthroscopy Drape, 85''x 96''
Reason
Latex content in product was labeled incorrectly as latex free.
Identifiers
| code_info | SKU Number 3601; Lot code/Expiration Date: Lot D181232, exp. 05/01/2022; Lot D181982, exp. 07/01/2022; Lot D202232, exp…SKU Number 3601; Lot code/Expiration Date: Lot D181232, exp. 05/01/2022; Lot D181982, exp. 07/01/2022; Lot D202232, exp.08/01/2024; Lot D210742, exp. 03/01/2025; Lot D211372, exp. 05/01/2025; Lot D212562, exp. 09/01/2025; Lot D213122, exp. 11/01/2025; and Lot D213402, exp. 12/01/2025. UDI: 50748426008556 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1071-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.