FDA Device recall Z-1273-2022
REF: PIG1260K, 6Fr, X10, Safe-t-Centesis Catheter drainage Kit, Sterile EO
- FDA Device
- Class II
- ongoing
- Published 2022-06-29
On 2022-06-29 the FDA classified a Class II recall of REF: PIG1260K, 6Fr, X10, Safe-t-Centesis Catheter drainage Kit, Sterile EO by Bard Peripheral Vascular, citing there is the potential that a 6 Fr Catheter Drainage kit contains an 8 Fr needle instead of a 6 Fr needle. They can be used in conjunction with the following drainage methods: Uni….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1273-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-04-22 |
| Published | 2022-06-29 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Bard Peripheral Vascular |
| Distribution | US |
Product
REF: PIG1260K, 6Fr, X10, Safe-t-Centesis Catheter drainage Kit, Sterile EO,
Reason
There is the potential that a 6 Fr Catheter Drainage kit contains an 8 Fr needle instead of a 6 Fr needle. They can be used in conjunction with the following drainage methods: Universal extension set and drainage bag, vacuum bottle, and wall suction.
Identifiers
| code_info | Lot # 0001405396; UDI/DI: (01)10885403076114 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
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All Bard Peripheral Vascular recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1273-2022%22
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