Curad Quick Strip fabric bandages recalled over compromised package seals
Medline is recalling 18,000 units of Curad Quick Strip Fabric Bandages because packaging may exhibit open seals that could compromise the sterility of the product.
The agency’s classification
FDA (Food): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The agency classified this recall as Class I — a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death. On that classification alone this is scored Severe; a score of Critical is reserved for recalls where a death or serious injury was reported. The agency gives the reason as: "Product tested positive Salmonella ."
Plain-English summary
Curad Quick Strip Fabric Bandages, containing 30 bandages of 3/4" x 3", Medline item number CUR1930P, are being recalled by Medline Industries, LP.
Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
The recall covers 18,000 units across all lots, carrying UDI/DI 10888277702776 for each, 00888277702779 for the box and 20888277702773 for the case. Distribution covered the United States, Guam, Canada and the United Arab Emirates. The FDA has classified the action as Class II.
A bandage whose sterile barrier is open may no longer be sterile when applied. The enforcement record reports no injuries. Customers should follow Medline's instructions.
The recalled product
- Product
- Deep-brand Select Arvi Net Wt. 12 oz. (340 g) KEEP FROZEN
- Manufacturer
- CHETAK NEW YORK LLC
- Category
- Medical Device — Wound dressing
- Affected units
- 3,509,532
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 (8)
- Lot: 25002
- 25031
- 25042
- 25063
- 25091
- 25132
- 25172
- 25196
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 52 recalled by CHETAK NEW YORK LLC under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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