First Aid Only Recalls Ibuprofen Dispenser Boxes Containing Aspirin
First Aid Only is recalling Smart Tab First Aid ezRefill System Ibuprofen boxes that were accidentally filled with aspirin packs.
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 Class II recall involving a packaging error where aspirin was placed in ibuprofen boxes. While this is a significant labeling/packaging error, the source does not report any illnesses or injuries, and the hazard is primarily related to incorrect medication identification rather than a high-risk pathogen or structural defect.
Plain-English summary
First Aid Only, Inc. is recalling Smart Tab First Aid ezRefill System Ibuprofen dispenser boxes (Item Number FAE 7014) and First Aid Cabinets containing these boxes. The recall involves 802 units of 20-count boxes distributed nationwide.
The recall was initiated because Ibuprofen boxes were accidentally used to package aspirin packs (10 packs of 2 / 235mg tablets). The affected boxes are coded B11340515, B11840515, B12040615, B12540615, B12640615, B12740615, C10340615, and B11040516.
Consumers should check their First Aid Cabinets for these specific Ibuprofen dispenser boxes. If the boxes contain aspirin packs instead of ibuprofen, they should stop using them and contact the manufacturer for instructions.
The recalled product
- Product
- Smart Tab First Aid ezRefill System Ibuprofen dispenser boxes (Item Number FAE 7014), 20 count boxes, First Aid Only Inc., Vancouver, WA
- Manufacturer
- First Aid Only Inc
- Affected units
- 802
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 (7)
- Aspirin was packed into Ibuprofen boxes (Item Number FAE-7014) coded: B11340515
- B11840515
- B12040615
- B12540615
- B12640615
- B12740615
- C10340615 and B11040516.
Distribution
Distributed nationwide across the United States.
Related recalls
Same hazard · mis labeling
See all →- ModerateMedline Trach Tube Kit Recalled for Component Labeling Discrepancy
FDA (Devices) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- ModerateOlympus Recalls PowerSeal Sealer Due to Incorrect Outer Box Labeling
FDA (Devices) · 2026-09-02
- HighSura Tanmen Ramen Noodles Recalled for Undeclared Fish Allergens
FDA (Food) · 2026-09-02
- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-09-02