Recall Z-1071-2022— Microtek Medical Inc.
Class II · Terminated
Class II FDA medical device recall by Microtek Medical Inc., initiated 2022-04-08, terminated 2024-06-05. FDA's recall record names no specific 510(k) clearance for this event. Product: TMJ Arthroscopy Drape, 85''x 96''. Reason: Latex content in product was labeled incorrectly as latex free..
- Recalling firm
- Microtek Medical Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2022-04-08
- Terminated
- 2024-06-05
- Firm location
- Saint Paul, MN, United States
Product description
TMJ Arthroscopy Drape, 85''x 96''
Reason for recall
Latex content in product was labeled incorrectly as latex free.
Data sourced from openFDA. This site is unofficial and independent of the FDA.