# FDA recall Z-2765-2026

> **Medline Industries, LP** · Class I · device recall initiated 2026-06-08.

## Product

MEDLINE medical procedure convenience kit labeled as:   1) TOTAL KNEE-LF, Medline kit SKU CDSOPT590T;  2) TOTAL KNEE-LF, Medline kit SKU CDSOPT590U;  3) TOTAL KNEE CDS, Medline kit SKU CDS983930J;  4) HIP CDS-LF, Medline kit SKU CDS984556L;  5) HIP CDS-LF, Medline kit SKU CDS984556M;  6) TOTAL KNEE PACK, Medline kit SKU DYNJ905162Q.

## 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.

## Distribution

US:  Mo, CO, IL

## Key facts

- **Recall number:** Z-2765-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-06-08
- **Report date:** 2026-07-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2765-2026

## Citation

> AI Analytics. FDA recall Z-2765-2026. Retrieved 2026-09-02 from https://api.ai-analytics.org/recall/Z-2765-2026. Source: US FDA. Licensed CC0.

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