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FDA Medical Device Recalls (openFDA)

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

Recall number
Z-1499-2023
Recalling firm
ASO LLC
Product
WALGREENS BANDAGES, item number 196568, 110 CT VALUE PACK, 24 BOXES/MASTER (shipping container), Walgreens Family Pack ASSORTED BANDAGES, 110 ASSORTED SIZES (retail package)
Status
Open, Classified
Initiated
2023-03-23
Posted
2023-05-02
Terminated
not on file
Reason
The adhesive bandage contains 0.1% benzalkonium chloride impregnated in the pad and is not disclosed on the labeling.
Root cause
Process design
Action
ASO sent an email to the headquarters of its sole consignee on 03/23/2023 to notify them of the intent to recall the product. The notice explained the issue and the risk and requested the return of the product from the retail level.
Quantity
919 cases of 24 units
Distribution
US Nationwide Distribution: IL. FL, CA, CT, OH, TX, IL, SC, and WI
Lot, serial or model codes
UDI/DI 311917124506; Lot Numbers: 00176259, 00176260, 00176582.
510(k) numbers
not on file
PMA numbers
not on file
Product code
KGX
Firm FEI
1038758
Firm city
Sarasota
Firm state
FL
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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