FDA Device recall Z-2947-2018
CIVCO Needle Guide, REF 676-150, QTY 24, STERILE EO
- FDA Device
- Class II
- terminated
- Published 2018-09-05
On 2018-09-05 the FDA classified a Class II recall of CIVCO Needle Guide, REF 676-150, QTY 24, STERILE EO by Civco Medical Instruments, citing the assembly of the needle guides were found to be either missing adhesive or did not have adequate adhesive to hold the assembled cannula in place on the needle guide.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2947-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-07-30 |
| Published | 2018-09-05 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Civco Medical Instruments |
| Distribution | n/a |
Product
CIVCO Needle Guide, REF 676-150, QTY 24, STERILE EO
Reason
The assembly of the needle guides were found to be either missing adhesive or did not have adequate adhesive to hold the assembled cannula in place on the needle guide.
Identifiers
| code_info | UDI 00841436107334, Lot numbers: A035054, A042207 |
|---|
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-2947-2018%22
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