Microtek Medical Inc. TMJ Arthroscopy Drape, 85''x 96'' Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
TMJ Arthroscopy Drape, 85''x 96''
Brand
Microtek Medical Inc.
Lot Codes / Batch Numbers
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
Products Sold
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
Microtek Medical Inc. is recalling TMJ Arthroscopy Drape, 85''x 96'' due to Latex content in product was labeled incorrectly as latex free.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Latex content in product was labeled incorrectly as latex free.
Recommended Action
Per FDA guidance
All consignees were contacted on 04/08/2022 via email. Consignees should read the recall instruction, examine their inventory, and quarantine the lots listed in the letter. The consignees should also complete the enclosed response form and email it to recall@ecolab.com. If the consignee has further distributed the product, they should identify and notify their customers of the recall.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026