TMJ Arthroscopy Drape recall
TMJ Arthroscopy Drape, 85''x 96''
Why was TMJ Arthroscopy Drape recalled?
Latex content in product was labeled incorrectly as latex free.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
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
- Product
- TMJ Arthroscopy Drape, 85''x 96''
- Recalling firm
- Microtek Medical Inc.
- Quantity
- 12 cases (120 drapes)
- Distribution
- Distributed nationwide to CO, PA, and WI.
- Recall date
- May 18, 2022
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)