# FDA recall Z-1127-2024

> **MEDLINE INDUSTRIES, LP - Northfield** · Class I · device recall initiated 2023-11-15.

## Product

Medline Kits, trays, and packs labeled as follows:    a) ANTERIOR PACK, REF DYNJ64814A;   b) ARTHROGRAM TRAY, REF DYNDH1629;   c) CVL INSERTION KIT-LF, REF DYNJ48587A;   d) EXTREMITY CDS, REF CDS983313I;   e) EXTREMITY CDS, REF DYNJ902004D;   f) EXTREMITY CDS, REF DYNJ902004F;   g) EXTREMITY IV, REF CMPJ06040D;   h) EXTREMITY IV, REF CMPJ06040F;   i) EXTREMITY PROCEDURE, REF CDS981656I;   j) FACIAL PLASTY PACK, REF DYNJ55335D;   k) FOOT PROCEDURE, REF CDS981659I;   l) FOOT PROCEDURE, REF CDS981659J;   m) HAND, REF DYNJ902002J;   n) HAND PACK, REF DYNJ35744A;   o) HAND PACK, REF DYNJ68873C;   p) HAND PACK, REF DYNJ46211K;   q) KNEE ARTHROSCOPY CDS, REF CDS941004C;   r) KNEE PACK, REF DYNJ68512;   s) LACERATION TRAY, REF SUT21580;   t) LOWER EXTREMITY, REF DYNJ907121F;   u) LOWER EXTREMITY, REF DYNJ46222M;   v) LOWER EXTREMITY PACK, REF DYNJ67216C;   w) LOWER EXTREMITY PACK, REF DYNJ67216D;   x) PACK,POSTERIOR SPINAL FUSION, REF DYNJ906892;   y) PODIATRY PACK, REF DYNJ68347A;   z) PODIAT

## Reason for recall

Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components):  0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.

## Distribution

Distribution US nationwide including Puerto Rico, Canada, UAE, and Panama

## Key facts

- **Recall number:** Z-1127-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-11-15
- **Report date:** 2024-03-06

- **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-1127-2024

## Citation

> AI Analytics. FDA recall Z-1127-2024. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-1127-2024. Source: US FDA. Licensed CC0.

---

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