ASO Recalls SHOPKO Waterproof Adhesive Pads Labeled as Antibacterial
ASO, LLC is recalling SHOPKO Waterproof Adhesive Pads because they were labeled as antibacterial but did not contain antibacterial ingredients.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: This is a labeling error where the product lacks the claimed antibacterial property, fitting the rubric for minor labeling errors or low-risk contamination without reported illness.
Plain-English summary
ASO, LLC is recalling SHOPKO Waterproof Adhesive Pads Antibacterial. These products are used for covering minor cuts, scrapes, and burns. The recall involves 37 cases, with 72 retail boxes in each case.
The reason for the recall is that no antibacterial bandages were packed in boxes labeled as antibacterial. This means the product did not contain the antibacterial properties claimed on the packaging.
The affected products were distributed in the states of Idaho, Wisconsin, Indiana, and Nebraska. The specific lot numbers are 330543 and 341383, and the UPC code is 400129133311. Consumers should check their bandages for these identifiers and stop using them if they match.
The recalled product
- Product
- SHOPKO Waterproof Adhesive Pads Antibacterial. Used for covering minor cuts, scrapes and burns.
- Manufacturer
- ASO, LLC
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- UPC Code #: 400129133311 Lot numbers: 330543 and 341383
Distribution
Related recalls
Same manufacturer · ASO, LLC
See all →- HighWalgreens assorted bandages recalled for undisclosed ingredient in adhesive
FDA (Devices) · 2023-05-10
- HighSterile Surgical Pads and Wound Care Kits Recalled Due to Structural Failure
FDA (Devices) · 2022-08-24
- HighFirst Aid Kits Recalled Due to Defective Acetaminophen
FDA (Devices) · 2022-05-11
- HighASO Recalls Family Wellness Sterile Gauze Pads Due to Sterilization Concerns
FDA (Devices) · 2018-12-12
- ModerateASO Recalls Carepak Bandages Due to Unlabeled Benzalkonium Chloride
FDA (Devices) · 2015-09-02
Same hazard · mis labeling
See all →- ModerateOlympus Recalls PowerSeal Sealer Due to Incorrect Outer Box Labeling
FDA (Devices) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- HighByron White A-L Complex Herbal Supplement Recalled for Undeclared Walnut
FDA (Food) · 2026-09-02
- ModerateMedline Trach Tube Kit Recalled for Component Labeling Discrepancy
FDA (Devices) · 2026-09-02
- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-09-02