FDA Device recall Z-0546-2014
Continuous Peripheral Nerve Block Catheter Kit and Set Continuous Peripheral Nerve Block Catheter Kit and Set permits placement of catheter…
- FDA Device
- Class II
- terminated
- Published 2013-12-25
On 2013-12-25 the FDA classified a Class II recall of Continuous Peripheral Nerve Block Catheter Kit and Set Continuous Peripheral Nerve Block Catheter Kit and Set permits placement of catheter… by Arrow International, citing A labeling inconsistency was discovered in which the lidstock states that the kit contains a stimulator cable with 1.5mm socket, however, the kit contains a stimulator cable with….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0546-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-10-09 |
| Published | 2013-12-25 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Arrow International |
| Distribution | US |
Product
Continuous Peripheral Nerve Block Catheter Kit and Set Continuous Peripheral Nerve Block Catheter Kit and Set permits placement of catheters next to nerves and nerve plexuses for continuous nerve block anesthesia or analgesia techniques for periods not exceeding 72 hours.
Reason
A labeling inconsistency was discovered in which the lidstock states that the kit contains a stimulator cable with 1.5mm socket, however, the kit contains a stimulator cable with 1.5mm pin.
Identifiers
| code_info | Product number AB-07200 Stimulator Adapter Cable with lot numbers: RF0059570, RF2069779, RF0088984, RF2108983, RF0128588, RF3052266, RF1071764. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Other recalls by Arrow International
- Description/REF: PI PICC: 3: 6FR x 55CM w CHG/ DLX-35563-HPKC
FDA Device · Class I · 2026-06-24 · Arrow International - Description/REF: BIOPSY SYSTEM COMPREHENSIVE KIT/ASK-09458-AH, ASK-09458-COC, ASK-09458-EUH, ASK-09458-SD, ASK-09458-VU
FDA Device · Class I · 2026-06-24 · Arrow International - Description/REF: HEMODIALYSIS KIT: 2L 14 FR X 20 CM AGB CDC-25142-X1A
FDA Device · Class I · 2026-06-24 · Arrow International - Description/REF: SAC KIT: 18 GA X 12CM W BIO/SAC-01218-B
FDA Device · Class I · 2026-06-24 · Arrow International - Description/REF: RA CATH KIT: 20 GA X 1-3/4IN/AK-04020-SPC
FDA Device · Class I · 2026-06-24 · Arrow International
All Arrow International recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0546-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.