Remel, Inc recalls remel BactiDrop Acridine Orange, REF 21502, 50 per package.
See all recalls from Remel, Inc →Recalled Product
remel BactiDrop Acridine Orange, REF 21502, 50 per package.
Hazard / Issue
A color change of the solution within the dropper can occur from orange-yellow to light yellow resulting in out-of-specification fluorescent stain results.
Issued by
FDA
Affected States: IL, IN, MN, NE, SD, TX, VA, WA
Lot/Code Info: Lot 733100, Exp. 2025-04-04; UDI-DI 848838000447.
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for remel BactiDrop Acridine Orange, →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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