Medline medical procedure convenience kits labeled as: 1) MEM… — Class II medical device recall Z-1192-2026
Ongoing recall by Medline Industries, LP, reported 2026-02-04, distributed nationwide. Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to c
| Recall number | Z-1192-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries, LP, Northfield, IL, United States |
| Recall initiated | 2025-12-12 |
| Classified | 2026-01-28 |
| Reported by FDA | 2026-02-04 |
| Distributed | Nationwide (US) |
| Quantity | 66 units |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 10195327056995, 10198459102257, 10198459359941, 10198459404009, 10198459423727, 10198459438820, 10653160990482, 10889942220083, 40195327056996, 40198459102258, 40198459359942, 40198459404000, 40198459423728, 40198459438821, 40653160990483, 40889942220084 |
| Lot numbers | 25JMJ958, 25KBE927, 25KMB767, 25KMD226, 25KME754, 25KMF183, 25KMG652, 25KMJ566, 25KMJ630 |
Product
Medline medical procedure convenience kits labeled as: 1) MEM MAXILLOFACIAL PACK-LF, Kit SKU DYNJ0660040R; 2) PLASTICS VCH, Kit SKU DYNJ39225K; 3) WT BREAST PACK, Kit SKU DYNJ46620I; 4) ENDO / AUG PACK, Kit SKU DYNJ59250I; 5) KMC PLASTIC/GEN PACK-LF, Kit SKU DYNJ65980J; 6) PLASTICS PACK, Kit SKU DYNJ68288A; 7) IMPLANT REMOVAL KIT, Kit SKU MNS13035; 8) PLASTICS PACK-LF, Kit SKU PHS41746D.
Reason for recall
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
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-1192-2026. 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.