Carepak Sheer Adhesive Bandages 50 Sterile Bandages Assorted Sizes
FDA device recall Z-2460-2015 · posted 2015-08-25 · Terminated
Recall details
- Recalling firm
- ASO, LLC
- Reason for recall
- Contain 0.1% Benzalkonium Chloride in the 5/8 bandages inside the assortment which is not listed as an active ingredient in the product label.
- Action taken
- Customers were contacted by phone and e-mail on 06/10/2015; First class letter was sent on 06/23/2015.
- Root cause
- Process control
- Status
- Terminated
- Product code
- KGX
- Quantity affected
- 655 cases.
- Distribution
- US Distribution to Rhode Island only
- Date initiated
- 2015-06-10
- Date posted
- 2015-08-25
- Date terminated
- 2016-10-12
- Location
- Sarasota, FL
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