CLASS II ONGOING Device recall · Reported 24 May 2017 · FDA Enforcement Report

White OR Towels, X-Ray Detectable, Sterile, 4 Towels per/pk;/Cs recalled

Medical Action Industries is recalling White OR Towels, X-Ray Detectable, Sterile, 4 Towels per/pk;/Cs. Intended for packing and, distributed in Arkansas, Indiana, Nevada. The recall was initiated on 19 Apr 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesMaterial Number: MSPT524, Lot #229445, Exp. Date: 10/12/2021.

Quantity recalled69 cases

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-2101-2017
FDA event ID: 77063
Recalling firm: Medical Action Industries, Arden, NC
Classification: Class II
Status: Ongoing
Recall initiated: 19 Apr 2017
FDA classified: 17 May 2017
Reported: 24 May 2017
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Sterility
Device type: Surgical Instruments

Timeline

19 Apr 2017	Recall initiated by company
17 May 2017	Classified by FDA	+28 days
24 May 2017	Published in enforcement report	+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Lint present on sterile Operating Room Towels.

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

White OR Towels, X-Ray Detectable, Sterile, 4 Towels per/pk; 20pk/Cs. Intended for packing and absorption externally or within patient wounds in various procedures or surgical cases.

Where it was distributed

AR, IN and NV.

Arkansas Indiana Nevada

Questions about this recall

Why was it recalled?

Lint present on sterile Operating Room Towels.

Which lots are affected?

Material Number: MSPT524, Lot #229445, Exp. Date: 10/12/2021.

Where was it sold?

AR, IN and NV.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 77063

Reported	Class	Recall	Company	Reason	Where
24 May 2017	CLASS II	Blue OR Towels, X-Ray Detectable, Sterile recalled	Medical Action Industries	Sterility	AR, IN, NV

More recalls from Medical Action Industries

All 14

Reported	Class	Recall	Company	Reason	Where
3 Apr 2019Device	CLASS II	Laparotomy Sponge with the following product description recalled	Medical Action Industries	Sterility	Nationwide
2 Jan 2019Device	CLASS II	Laparotomy Sponge, XR No Loop, Single-Use, Sterile recalled	Medical Action Industries	Sterility	5 states
6 Jun 2018Device	CLASS II	Blue OR Towel Non X-Ray Detectable recalled by Medical Action Industries	Medical Action Industries	Sterility	7 states
24 May 2017Device	CLASS II	Blue OR Towels, X-Ray Detectable, Sterile recalled	Medical Action Industries	Sterility	AR, IN, NV
9 Mar 2016Device	CLASS II	PICC/CVC Secure Dressing Change kit recalled	Medical Action Industries	Labeling Errors	Nationwide

Other Surgical Instruments recalls

All 3,809

Reported	Class	Recall	Company	Reason	Where
9 Sep 2026Device	CLASS II	Medline Convenience Kits: IV Start KIT recalled by Medline Industries	Medline Industries	Sterility	Nationwide
9 Sep 2026Device	CLASS II	Medline Convenience Kits containing BD ChloraPrep Clear recalled	Medline Industries	Packaging Defects	Nationwide
2 Sep 2026Device	CLASS II	Medline convenience kits labeled as: Open Heart Pack, Medline Kit recalled	Medline Industries	Other	Nationwide
2 Sep 2026Device	CLASS II	Medline convenience kits labeled as: GYN Robotic CDS, Medline Kit recalled	Medline Industries	Other	Nationwide
2 Sep 2026Device	CLASS II	Linvatec Genesys CrossFT Suture Anchor with Disposable Driver recalled	ConMed	Other	Nationwide