Device recall
Z-0183-2026: Medical convenience kits Item Number/Description HSLM53AB SPINE PACK MILM82A DTC…
FDA device recall · Class II · American Contract Systems Inc.
Key facts
| Recall number (Z-number) | Z-0183-2026 |
|---|---|
| Recall event | 97659 |
| Product | Medical convenience kits Item Number/Description HSLM53AB SPINE PACK MILM82A DTC LAMINECTOMY PACK (PS 209475) RCNA47B NEURO ANGIO 0246971 SFLM54AB LAMINECTOMY PACK - 219659 UDLM94AA LAMINECTOMY PACK - 206064 UILM77AU LAMINECTOMY (PS 039500) UINR44P NEURO IR PERIPHERAL (PS 64405) UISH15AV SHUNT PACK… |
| Product code | OJG |
| Recalling firm | American Contract Systems Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3007069947 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database