Stryker Sustainability Solutions Recall 92138
Description: REF 5065, Kendall, Impad Rigid Sole Foot Cover, Regular Pair ,<12", Rx Only Non-Sterile
Stryker Sustainability Solutions Recall 92138 Information
| Status | Ongoing |
| Mandated? | Voluntary: Firm initiated |
| Recall Number | Z-1612-2023 |
| Event ID | 92138 |
| Event Description | REF 5065, Kendall, Impad Rigid Sole Foot Cover, Regular Pair ,<12", Rx Only Non-Sterile |
| Product Type | Devices |
| Distribution | US: WA OUS: None |
| Quantity | 50 units |
| Recall Reason | Through complaint surveillance, it was identified that reprocessed Deep vein thrombosis (DVT) Compression Sleeves may be mislabeled and/or mispackaged. |
| Device Classification | 20230524 |
| Device Code Info | Lot # 0000157564, UDI-DI: 00885825013585 |
| Center Classification Date | 20230519 |
| Recall Initiation Date | 20230414 |
| Recalling Firm | Stryker Sustainability Solutions |
| Initial Notification | |
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