CLASS II ONGOING Device recall · Reported 10 May 2023 · FDA Enforcement Report

Walgreens Bandages recalled by ASO

ASO is recalling Walgreens Bandages, distributed nationwide in the US. The recall was initiated on 23 Mar 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesUDI/DI 311917124506; Lot Numbers: 00176259, 00176260, 00176582.

Quantity recalled919 cases of 24 units

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-1499-2023
FDA event ID: 91970
Recalling firm: ASO, Sarasota, FL
Classification: Class II
Status: Ongoing
Recall initiated: 23 Mar 2023
FDA classified: 2 May 2023
Reported: 10 May 2023
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Packaging Defects
Device type: Hip & Knee Implants

Timeline

23 Mar 2023	Recall initiated by company
2 May 2023	Classified by FDA	+40 days
10 May 2023	Published in enforcement report	+8 days

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

Reason for recall

The adhesive bandage contains 0.1% benzalkonium chloride impregnated in the pad and is not disclosed on the labeling.

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

WALGREENS BANDAGES, item number 196568, 110 CT VALUE PACK, 24 BOXES/MASTER (shipping container), Walgreens Family Pack ASSORTED BANDAGES, 110 ASSORTED SIZES (retail package)

Where it was distributed

US Nationwide Distribution: IL. FL, CA, CT, OH, TX, IL, SC, and WI

Nationwide California Connecticut Florida Illinois Ohio South Carolina Texas Wisconsin

Stores named: Walgreens

Questions about this recall

Why was it recalled?

The adhesive bandage contains 0.1% benzalkonium chloride impregnated in the pad and is not disclosed on the labeling.

Which lots are affected?

UDI/DI 311917124506; Lot Numbers: 00176259, 00176260, 00176582.

Where was it sold?

US Nationwide Distribution: IL. FL, CA, CT, OH, TX, IL, SC, and WI

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.

More recalls from ASO

All 15

Reported	Class	Recall	Company	Reason	Where
24 Aug 2022Device	CLASS II	CVS Health Sterile Surgical Pads, Cushion Comfort, packaged 12 pads recalled	ASO	Packaging Defects	Nationwide
11 May 2022Device	CLASS II	First Aid Kits containing acetaminophen under brand names recalledacetaminophen under	ASO	Other	Nationwide
12 Dec 2018Device	CLASS II	Family Wellness First Aid Sterile Gauze Pad White, bleached recalled	ASO	Device Malfunction	Nationwide
2 Sep 2015Device	CLASS II	Carepak Sheer Adhesive Bandages 50 Sterile Bandages Assorted Sizes recalled	ASO	Other	RI
9 Oct 2013Device	CLASS II	Shopko Waterproof Adhesive Pads Antibacterial recalled by ASO	ASO	Other	IN, NE, WI

Other Hip & Knee Implants recalls

All 3,110

Reported	Class	Recall	Company	Reason	Where
30 Sep 2026Device	CLASS II	Trinity Non-Surgical Isolation Gown, AAMI PB70 Level 2, X-Large recalled	New York Embroidery Studio	Packaging Defects	Nationwide
23 Sep 2026Device	CLASS II	Axle Pin Assy Large Elbow Cobalt Chrome recalled by Howmedica Osteonics	Howmedica Osteonics	Other	Nationwide
23 Sep 2026Device	CLASS II	Triathlon Hinge Insert Size 4 5612-p-411 Triathlon Hinge recalled	Howmedica Osteonics	Other	Nationwide
23 Sep 2026Device	CLASS II	Scorpio Recessed Metal Backed Patella 3045 recalled	Howmedica Osteonics	Foreign Material	Nationwide
23 Sep 2026Device	CLASS II	Bearing And Axle Bushing Assy Std Elbow C-m113-1-301 Krh recalled	Howmedica Osteonics	Other	Nationwide