FDA Device recall Z-0881-2017
K-Wire 1.4mm x 12in Non-Threaded, Part Number 9080-12U
- FDA Device
- Class II
- terminated
- Published 2016-12-28
On 2016-12-28 the FDA classified a Class II recall of K-Wire 1.4mm x 12in Non-Threaded, Part Number 9080-12U by Amendia, citing the rods are packaged in packages with unacceptable seals. In some cases, the integrity of the seal is compromised by channels or voids.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0881-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-11-22 |
| Published | 2016-12-28 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Amendia |
| Distribution | US |
Product
K-Wire 1.4mm x 12in Non-Threaded, Part Number 9080-12U; K-Wire Threaded 1.4mm x 18, Part Number 9080-18T; K-Wire Non-Threaded 1.4mm x 18, Part Number 9080-18U; 1.4mm x 24 Threaded Guide Wire, Part Number 9080-24T; K-Wire Non-Threaded 24, Part Number 9080-24U; Blunt K-Wire, 18 inches, Threaded, Part Number 9080B-18T; Blunt K-Wire, 18 inches, Unthreaded, Part Number 9080B-18U; Blunt K-Wire, 24 inches, Unthreaded, Part Number 9080B-24U; 1.4mm x 18 Blunt Threaded Nitinol Guide Wire, Part Number 9080B-N-18T; 1.4mm x 18" Blunt Non-Threaded Nitinol Guide Wire, Part Number 9080B-N-18U; Lodestar K-wire Non-Threaded, 18, Part Number 9080L-18U; 1.4mm x 18 Threaded Nitinol Guide Wire, Part Number 9080-N-18T; 1.4mm x 18 Non-Threaded Nitinol Guide Wire, Part Number 9080-N-18U The guide wire is passed through the cannulated handle of the Dual Stylet Needles and pressed into the bone
Reason
The rods are packaged in packages with unacceptable seals. In some cases, the integrity of the seal is compromised by channels or voids.
Identifiers
| code_info | Part Number 9080-12U Lot Number 121306, 121307, 122628, 122721, 124400, 132732, 135403; Part Number 9080-18T Lot Numb…Part Number 9080-12U Lot Number 121306, 121307, 122628, 122721, 124400, 132732, 135403; Part Number 9080-18T Lot Number 122486, 122626, 123957, 124408, 127435, 129132, 129803, 129935, 131072, 135560, 135566, 135567; Part Number 9080-18U Lot Number 122470, 123948, 129802, 129936, 130390, 130391, 131073; Part Number 9080-24T Lot Number 133359; Part Number 9080-24U Lot Number 134108, 134112, 134908; Part Number 9080B-18T Lot Number 124547, 126820, 127437, 131454, 132592, 134181, 135401; Part Number 9080B-18U Lot Number 122468, 123938, 126504, 127436, 129800, 130947, 131453, 132750, 133645, 134169, 134907, 135563, 135578, 135579, 135580; Part Number 9080B-24U Lot Number 122239, 130392, 130393, 131839, 133988, 135359, 135360, 135400; Part Number 9080B-N-18T Lot Number 124137, 125331, 128472, 130612, 132229, 135584, 135585, 137464; Part Number 9080B-N-18U Lot Number 123556, 125199, 126821, 128348, 128469, 129443, 129915, 130836, 131626, 133118, 134180, 135208; Part Number 9080L-18U |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0881-2017%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.