FDA Device recall Z-0935-2019
Phoenix AP AST Indicator Bag, Catalog Number 246006
- FDA Device
- Class II
- terminated
- Published 2019-03-06
On 2019-03-06 the FDA classified a Class II recall of Phoenix AP AST Indicator Bag, Catalog Number 246006 by Becton Dickinson And, citing panels inoculated using certain lots of the indicator solution are demonstrating an increased occurrence of test aborts.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0935-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-12-20 |
| Published | 2019-03-06 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Becton Dickinson And |
| Distribution | AL, AR, AZ, CA, CO, CT, DC, FL, GA, IA, ID, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV, WY |
Product
Phoenix AP AST Indicator Bag, Catalog Number 246006
Reason
Panels inoculated using certain lots of the indicator solution are demonstrating an increased occurrence of test aborts.
Identifiers
| code_info | Batch Numbers 8234684 8234533 8225579 8225578 8218607 8218605 8213696 8213635 8213633 8208581 8208579 820658…Batch Numbers 8234684 8234533 8225579 8225578 8218607 8218605 8213696 8213635 8213633 8208581 8208579 8206585 8190531 8190530 8170557 8234505 8170562 8159691 8150670 8150669 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0935-2019%22
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