FDA Device recall Z-2102-2017
Blue OR Towels, X-Ray Detectable, Sterile, 2 Towels per/pk
- FDA Device
- Class II
- ongoing
- Published 2017-05-24
On 2017-05-24 the FDA classified a Class II recall of Blue OR Towels, X-Ray Detectable, Sterile, 2 Towels per/pk by Medical Action Industries, citing lint present on sterile Operating Room Towels.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2102-2017 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2017-04-19 |
| Published | 2017-05-24 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Medical Action Industries |
| Distribution | AR, IN, NV |
Product
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
Lint present on sterile Operating Room Towels.
Identifiers
| code_info | 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). |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2102-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.