# FDA recall Z-3121-2024

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-06-27.

## Product

Medline convenience kits containing semi-rigid suction liners labeled as follows:  a) LAMINECTOMY CDS, Pack Number CDS981510L;   b) ORTHO TRAUMA-LF, Pack Number DYNJ900720D;   c) ORTHO TRAUMA-LF, Pack Number DYNJ900720F;   d) KNEE ARTHROSCOPY, Pack Number DYNJ908090C;   e) LAMINECTOMY, Pack Number DYNJ908091B;   f) PODIATRY, Pack Number DYNJ908092C;   g) ANTERIOR TOTAL HIP, Pack Number DYNJ908095B;   h) CRANI, Pack Number DYNJ908097A;   i) HIP PINNING, Pack Number DYNJ908102B;   j) (76) LOWER EXTREMITY, Pack Number DYNJ908103B;   k) SHOULDER ARTHROSCOPY, Pack Number DYNJ908110B;   m) HAND-LF, Pack Number DYNJ908425;   n) TOTAL JOINT, Pack Number DYNJ908660A;   o) MERCY TIFFIN HAND, Pack Number DYNJ909734;   p) MERCY TIFFIN TOTAL KNEE, Pack Number DYNJ909738;   q) MTHZ KNEE ARTHROSCOPY, Pack Number DYNJ909740;   r) ACL-WHSC, Pack Number DYNJ910074A;   s) EXTREMITY-WHSC, Pack Number DYNJ910077;   t) EXTREMITY-WHSC, Pack Number DYNJ910077A;   u) KNEE ARTHROSCOPY-WHSC, Pack Number DYNJ9100

## Reason for recall

Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.

## Distribution

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

## Key facts

- **Recall number:** Z-3121-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-27
- **Report date:** 2024-09-18

- **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-3121-2024

## Citation

> AI Analytics. FDA recall Z-3121-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-3121-2024. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*