Medline brand medical procedure convenience kits — Class II medical device recall Z-0179-2025
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-10-30, distributed nationwide. It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may re
| Recall number | Z-0179-2025 |
|---|---|
| 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 | 2024-09-04 |
| Classified | 2024-10-23 |
| Reported by FDA | 2024-10-30 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, PA |
| Quantity | 2,371 units |
| Reason classes | sterility, packaging |
| UPC / GTIN / UDI-DI | 10193489221053, 10193489225587, 10193489361667, 10193489373592, 10193489695823, 10193489760484, 10195327235413, 10195327246747, 10195327296407, 10195327389970, 10195327399702, 10195327433963, 10195327456672, 10195327509903, 10195327543082, 10195327582036, 10195327609726, 10888277002890, 10889942279302, 10889942313105, 10889942314317, 10889942686612, 10889942791767, 10889942848447, 10889942919222 and 25 more |
| Lot numbers | 23KBB893, 23KBE137, 23KBE944, 23KBO606, 23LBK801, 23LBL852, 23LBL961, 23LBO084, 23LBO506, 23LBO732, 23LBP194, 23LBS030, 23LBS071, 23LBV189, 23LBV377, 24ABB592, 24ABD667, 24ABG182, 24ABG221, 24ABG354, 24ABG603, 24ABG702, 24ABK563, 24ABW931, 24BBC876, 24BBF009, 24BBQ775 |
| Model numbers | CDS982519W, CDS984003A, DYNJ32639C, DYNJ39547B, DYNJ41229C, DYNJ45153B, DYNJ46719B, DYNJ46739B, DYNJ48587A, DYNJ48892C, DYNJ49301B, DYNJ50952F, DYNJ51383F, DYNJ54602A, DYNJ55324G, DYNJ58115A, DYNJ62877, DYNJ64823, DYNJ83675, DYNJ85288A, DYNJ85503, DYNJ909569, YNJ10253B, YNJ910003A, YNJ910004C |
Product
Medline brand medical procedure convenience kits, labeled as: 1) NEW LONDON TOTAL KNEE CDS, REF CDS982519W; 2) HAND/FOOT CDS, REF CDS984003A; 3) SPECIAL PROCEDURE PACK, REF DYNJ32639C; 4) PK-ORTHO-MINOR, REF DYNJ39547B; 5) ANT CERV ADD ON PACK, REF DYNJ41229C; 6) NAVIGATIONAL SPINE FUSION, REF DYNJ45153B; 7) FEET, ELBOW, AND ANKLE TEGH-LF, REF DYNJ46719B; 8) PLASTIC HAND PACK TEGH-LF, REF DYNJ46739B; 9) CVL INSERTION KIT-LF, REF DYNJ48587A; 10) CVL INSERTION KIT-LF, REF DYNJ48587A; 11) ENSEMBLE SURPLUS LCA-LF, REF DYNJ48892C; 12) EXTREMITY PACK, REF DYNJ49301B; 13) ACL ACCESSORY PACK, REF DYNJ50952F; 14) SPINAL INJECTION PACK, REF DYNJ51383F; 15) FTMC ARTHROS BASIC SETUP-LF, REF DYNJ54602A; 16) MINOR EXTREMITY PACK, REF DYNJ55324G; 17) MINOR EXTREMITY PACK, REF DYNJ55324G; 18) D-SPINE SUPPLEMENT PACK, REF DYNJ58115A; 19) EXTREMITY PACK, REF DYNJ62877; 20) AHT LG KNEE ROLL, REF DYNJ64823; 21) CUSTOM ORTHO PACK, REF DYNJ83675; 22) DR SUNDAR SCS KIT, REF DYNJ85288A; 23) CENTRAL SCS TRIAL PACK, REF DYNJ85503; 24) TOTAL KNEE CDS-LF, REF DYNJ909569; 25) EXTREMITY PACK, REF SYNJ10253B; 26) CARROLLTON HIP FX, REF SYNJ910003A; 27) ARTHROSCOPY, REF SYNJ910004C
Reason for recall
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
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-0179-2025. 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.