PlainRecalls
FDA Devices Moderate Class II Terminated

TMJ Arthroscopy Drape, 85''x 96''

Reported: May 18, 2022 Initiated: April 8, 2022 #Z-1071-2022

Product Description

TMJ Arthroscopy Drape, 85''x 96''

Reason for Recall

Latex content in product was labeled incorrectly as latex free.

Details

Recalling Firm
Microtek Medical Inc.
Units Affected
12 cases (120 drapes)
Distribution
Distributed nationwide to CO, PA, and WI.
Location
Saint Paul, MN

Frequently Asked Questions

What product was recalled?
TMJ Arthroscopy Drape, 85''x 96''. Recalled by Microtek Medical Inc.. Units affected: 12 cases (120 drapes).
Why was this product recalled?
Latex content in product was labeled incorrectly as latex free.
Which agency issued this recall?
This recall was issued by the FDA Devices on May 18, 2022. Severity: Moderate. Recall number: Z-1071-2022.