# FDA recall Z-2283-2025

> **Carefree Surgical Specialties** · Class II · device recall initiated 2025-07-01.

## Product

Brand Name: Carefree Surgical Specialties  Product Name: Robotic/Laparoscopy Kittner Rolls Gauze Medium 4  Long  X-Ray Detectable 5/pk 25pk/CS  Model/Catalog Number: 15505/25  Product Description: Robotic/Laparoscopy Kittner Rolls Gauze Medium 4  Long  X-Ray Detectable 5/pk 25pk/CS

## Reason for recall

Due to two issues:  1. Product contamination (biological foreign matter) that could compromise sterility.  2. Incorrect quantity of gauze in sterile packaging

## Distribution

US Nationwide distribution in the states of KY, TX, FL, NC, CO, CA, ID, WV, NY, IL, IN, IA, MI, LA, WI, MT, VA, MA, TN, CT, AL, PA, MO, NJ, AR, OH, NE, AZ, MN, MD, GA, NC, WA, VT, OK, RI, SC, NH, VT, NV, OR.

## Key facts

- **Recall number:** Z-2283-2025
- **Recalling firm:** Carefree Surgical Specialties
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-07-01
- **Report date:** 2025-08-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Nampa, ID, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2283-2025

## Citation

> AI Analytics. FDA recall Z-2283-2025. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2283-2025. Source: US FDA. Licensed CC0.

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