Z-2102-2017 Class II Ongoing
FDA device recall Z-2102-2017 was initiated by Medical Action Industries Inc on April 19, 2017 and is designated Class II. Reason for recall: Lint present on sterile Operating Room Towels. The recall status is ongoing. Affected quantity: 38 cases (3-48pk/35-20pk).
Recall Details
- Product Type
- Devices
- Report Date
- May 24, 2017
- Initiation Date
- April 19, 2017
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 38 cases (3-48pk/35-20pk)
Product Description
Blue OR Towels, X-Ray Detectable, Sterile, 2 Towels per/pk; 48pk/Cs and 4 Towels per/pk; (20pk/Cs). Intended for packing and absorption externally or within patient wounds in various procedures or surgical cases.
Reason for Recall
Lint present on sterile Operating Room Towels.
Distribution Pattern
AR, IN and NV.
Code Information
Material Number: AVID260, Lot #231253, Exp. Date: 10/31/2021 (48 pk) and Material Number: MSPT504, Lot #229259, Exp. Date: 10/12/2021 (20 pk).