MEDLINE medical procedure convenience kit labeled as: HIP CDS-LF — Class I medical device recall Z-2764-2026
Ongoing recall by Medline Industries, LP, reported 2026-07-29, distributed in CO, IL. The procedure kits contain ICU Medical, Inc. pain management kits containing Bupivacaine Hydrochloride in Dext
| Recall number | Z-2764-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries, LP, Northfield, IL, United States |
| Recall initiated | 2026-06-08 |
| Classified | 2026-07-22 |
| Reported by FDA | 2026-07-29 |
| Distributed | CO, IL |
| Quantity | 52 kits |
| UPC / GTIN / UDI-DI | 10198459266621, 40198459266622 |
| Lot numbers | 25GDA213, 25KDB472, 26ADA161, 26ADB079, 26BDB740, 26DDA718, 26EDA285 |
Product
MEDLINE medical procedure convenience kit labeled as: HIP CDS-LF, Medline kit SKU CDS984556N
Reason for recall
The procedure kits contain ICU Medical, Inc. pain management kits containing Bupivacaine Hydrochloride in Dextrose Injection, USP, which were recalled due to quality issues that could result in drug ineffectiveness.
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-2764-2026. 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.