# FDA recall Z-1086-2026

> **Medline Industries, LP** · Class II · device recall initiated 2025-12-16.

## Product

Medline medical procedure convenience kits labeled as:    1) LAPAROSCOPY CDS-LF, REF CDS860235L;   2) GENERAL LAPAROSCOPIC, REF CDS930223M;   3) LAP CHOLE CDS, REF CDS983678K;   4) LAPAROSCOPY PELV CDS, REF CDS983679K;   5) LAP CHOLE CDS-LF, REF CDS983752M;   6) LAP CHOLE CDS-LF, REF CDS984016B;   7) LAP CHOLE KIT, REF CDS984020P;   8) LAP CHOLE-LF, REF CDS984175J;   9) LAP COLON CDS, REF CDS984849N;   10) GENERAL LAPAROSCOPY CDS, REF CDS985328M;   11) LAP CHOLE, REF DYNJQ9044O;   12) GENERAL LAPAROSCOPY V, REF DYNJS2032F;   13) LAP CHOLE PACK, REF DYNJ26209R;   14) LAP CHOLE PACK, REF DYNJ26209S;   15) GENERAL LAPAROSCOPY PACK, REF DYNJ37459D;   16) DR. BROWN LAP CHOLE PLUS SETUP, REF DYNJ42578G;   17) LAPAROSCOPY GENERAL PACK, REF DYNJ45083G;   18) LAP CHOLE PACK, REF DYNJ51785D;   19) LAPAROSCOPY PACK, REF DYNJ61652A;   20) ENDOSCOPY, REF DYNJ62133A;   21) LAP CHOLE PACK, REF DYNJ66285A;   22) LAPAROSCOPY PACK, REF DYNJ66289B;   23) LAPAROSCOPIC CHOLECYSTECTO, REF DYNJ67296D;   24) 

## Reason for recall

Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and battery pack during use of the Strykeflow 2 Suction Irrigator. This design change has caused some devices to leak and/or emit vaporized saline (which can resemble smoke) during use.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1086-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-12-16
- **Report date:** 2026-01-21

- **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-1086-2026

## Citation

> AI Analytics. FDA recall Z-1086-2026. Retrieved 2026-07-07 from https://api.ai-analytics.org/recall/Z-1086-2026. Source: US FDA. Licensed CC0.

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