# FDA recall Z-0179-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-09-04.

## Product

Medline brand medical procedure convenience kits, labeled as:    1) NEW LONDON TOTAL KNEE CDS, REF CDS982519W;   2) HAND/FOOT CDS, REF CDS984003A;   3) SPECIAL PROCEDURE PACK, REF DYNJ32639C;   4) PK-ORTHO-MINOR, REF DYNJ39547B;   5) ANT CERV ADD ON PACK, REF DYNJ41229C;   6) NAVIGATIONAL SPINE FUSION, REF DYNJ45153B;   7) FEET, ELBOW, AND ANKLE TEGH-LF, REF DYNJ46719B;   8) PLASTIC HAND PACK TEGH-LF, REF DYNJ46739B;   9) CVL INSERTION KIT-LF, REF DYNJ48587A;   10) CVL INSERTION KIT-LF, REF DYNJ48587A;   11) ENSEMBLE SURPLUS LCA-LF, REF DYNJ48892C;   12) EXTREMITY PACK, REF DYNJ49301B;   13) ACL ACCESSORY PACK, REF DYNJ50952F;   14) SPINAL INJECTION PACK, REF DYNJ51383F;   15) FTMC ARTHROS BASIC SETUP-LF, REF DYNJ54602A;   16) MINOR EXTREMITY PACK, REF DYNJ55324G;   17) MINOR EXTREMITY PACK, REF DYNJ55324G;   18) D-SPINE SUPPLEMENT PACK, REF DYNJ58115A;   19) EXTREMITY PACK, REF DYNJ62877;   20) AHT LG KNEE ROLL, REF DYNJ64823;   21) CUSTOM ORTHO PACK, REF DYNJ83675;   22) DR SUNDAR SC

## Reason for recall

It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Panama.

## Key facts

- **Recall number:** Z-0179-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-09-04
- **Report date:** 2024-10-30

- **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-0179-2025

## Citation

> AI Analytics. FDA recall Z-0179-2025. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0179-2025. Source: US FDA. Licensed CC0.

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