PlainRecalls
FDA Devices Moderate Class II Ongoing

remel BactiDrop Acridine Orange, REF 21502, 50 per package.

Reported: November 6, 2024 Initiated: September 20, 2024 #Z-0266-2025

Product Description

remel BactiDrop Acridine Orange, REF 21502, 50 per package.

Reason for Recall

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.

Details

Recalling Firm
Remel, Inc
Units Affected
29 kits
Distribution
Distribution was made to IL, IN, MN, NE, SD, TX, VA, and WA. There was government distribution but no military distribution. Foreign distribution was made to the United Kingdom.
Location
Lenexa, KS

Frequently Asked Questions

What product was recalled?
remel BactiDrop Acridine Orange, REF 21502, 50 per package.. Recalled by Remel, Inc. Units affected: 29 kits.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 6, 2024. Severity: Moderate. Recall number: Z-0266-2025.