Medline HOI LUMBAR REF DYNJ902823G Lot 20AKA895 Expiration 2021-05-31… — Class II medical device recall Z-1357-2020
Terminated recall by Medline Industries Inc, reported 2020-03-04, distributed in CA. The sterile pack inside the Complete Delivery System (CDS) did not go through a complete sterilization cycle,
| Recall number | Z-1357-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries Inc, Northfield, IL, United States |
| Recall initiated | 2020-01-21 |
| Classified | 2020-02-25 |
| Reported by FDA | 2020-03-04 |
| Terminated | 2023-01-12 |
| Distributed | CA |
| Quantity | 122 |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 10193489219180 |
| Lot numbers | 20AKA895 |
| Model numbers | DYNJ902823G |
| Expiration dates | 2021-05-31 |
Product
Medline HOI LUMBAR REF DYNJ902823G Lot 20AKA895 Expiration 2021-05-31 1 each GTIN (01)10193489219180
Reason for recall
The sterile pack inside the Complete Delivery System (CDS) did not go through a complete sterilization cycle, therefore the sterility of these components cannot be guaranteed.
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-1357-2020. 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.