# Class II recall Z-0183-2027: Medline Industries, LP

**Predicate Speed & CAPA Advisory Opportunity Score:** 62/100

| Field | Value |
|---|---|
| Record | Device recall |
| Recall number | Z-0183-2027 |
| Recalling firm | Medline Industries, LP |
| Classification | Class II |
| Status | Ongoing |
| Voluntary / mandated | Voluntary: Firm initiated |
| Specialty | Other |
| Product | Convenience Kits containing CONMED AirSeal Access Ports    CHN GYN ONCOLOGY	  	DYNJ906731K          DYNJ906731L  	DYNJ906731N  	  DAVINCI PROSTATECTOMY	  	DYNJG901002A  	  	  	DYNJG901002B          DYNJG901002C  	DYNJG901002D    GENERAL DAVINCI	  	DYNJG901004B  	DYNJG901004D    HERNANDEZ DAVINCI ACC BUNDLE M	  	DYNJ911258A  	  KIT ROBOTICS UROLOGY PROSTATE	  	DYKMBNDL116D  	DYKMBNDL116F  	  ROBOTIC GYN	  	DYNJ907827F  	  ROBOTIC PACK	  	DYNJ50474G    RR-DAVINCI PROSTATE ACCESSORY	  	DYNJ63392C          DYNJ63392F |
| Reason | Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures. |
| Quantity | 3,551 kits |
| Distribution | US Nationwide distribution in the states of AZ, CA, IN, MD, MO, NJ, OH, and WI. |
| Recall initiated | 2026-08-31 |
| Reported | 2026-10-21 |
| Firm location | Northfield, IL, United States |

## Why this score
- Class II recall: usually triggers CAPA and quality-system remediation work.
- Recall is still ongoing.
- Posted 15 days ago.

Source: U.S. FDA openFDA (510(k) clearances and device enforcement reports) (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0183-2027%22). Last refreshed: 2026-11-04T21:30:53.898Z.
Data from the FDA openFDA API, which may lag official FDA databases. Informational only; not regulatory or legal advice.