Surgical convenience kits labeled as: MEDLINE SHOULDER SUSPENSION I-LF — Class II medical device recall Z-1122-2023
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2023-02-22, distributed nationwide. The recall is due to the perforated bag not allowing for outside of the kit wrapping to be sterile, therefore,
| Recall number | Z-1122-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2022-12-07 |
| Classified | 2023-02-10 |
| Reported by FDA | 2023-02-22 |
| Distributed | Nationwide (US) |
| Quantity | 1,280 units |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 10080196597383 |
| Lot numbers | 22DBN321 |
Product
Surgical convenience kits labeled as: MEDLINE SHOULDER SUSPENSION I-LF, Reorder Number DYNJSHOULDER
Reason for recall
The recall is due to the perforated bag not allowing for outside of the kit wrapping to be sterile, therefore, only the contents inside the kits wrapping are sterile.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1122-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.