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FDA Medical Device Recalls (openFDA)

Medical Action Industries Inc: 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.

Recall number
Z-2102-2017
Recalling firm
Medical Action Industries Inc
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.
Status
Open, Classified
Initiated
2017-04-19
Posted
not on file
Terminated
not on file
Reason
Lint present on sterile Operating Room Towels.
Root cause
Other
Action
Consignees were notified via Medical Device Notification of Recall notice on/about 4/19/2017.
Quantity
38 cases (3-48pk/35-20pk)
Distribution
AR, IN and NV.
Lot, serial or model codes
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).
510(k) numbers
not on file
PMA numbers
not on file
Product code
GDY
Firm FEI
1030451
Firm city
Arden
Firm state
NC
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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