FDA Device recall Z-2868-2016
PHS Spinal Tray 24G Gertie Marx, Catalogue No. 899379
- FDA Device
- Class II
- terminated
- Published 2016-09-28
On 2016-09-28 the FDA classified a Class II recall of PHS Spinal Tray 24G Gertie Marx, Catalogue No. 899379 by Integra Lifesciences D B A Integra Pain Management, citing integra LifeSciences has recently identified that one lot of Spinal Tray 24 G Gertie Marx Catalogue # 899379 was shipped containing the 24 G Gertie Marx needle without an introduc….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2868-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-08-24 |
| Published | 2016-09-28 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Integra Lifesciences D B A Integra Pain Management |
| Distribution | CA |
Product
PHS Spinal Tray 24G Gertie Marx, Catalogue No. 899379. Intended to provide licensed medical professionals with a kit containing drugs and other medical devices that are used to support the administration of general, local anesthetics.
Reason
Integra LifeSciences has recently identified that one lot of Spinal Tray 24 G Gertie Marx Catalogue # 899379 was shipped containing the 24 G Gertie Marx needle without an introducer.
Identifiers
| code_info | Lot Number affected: W1503532 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2868-2016%22
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