# FDA recall Z-0166-2025

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

## Product

Medline brand medical procedure convenience kits, labeled as: 1) THORACENTESIS TRAY, REF 00-400616J;  2) HH PACK SONICATION SPEC CONTAI, REF 3706WHST;  3) T&A CDS, REF CDS980427J;  4) EVD CDS, REF CDS984603;  5) CHEST DRAINAGE TRAY, REF CHT745;  6) TRAY FOL TEMP  UM 14FR 10ML MF, REF DYND150814TS;  7) TRAY FOL TEMP  UM 14FR 10ML MF, REF DYND150814TS;  8) CUSTOM KIT, REF DYNDA2060;  9) CHEST TRAY PACK, REF DYNDA2203;  10) PK LESION CSTM, REF DYNDA2914;  11) BRONCH ESOPHAGOSCOPY PACK, REF DYNDH1765;  12) SOFT TISSUE PACK, REF DYNJ00017M;  13) M1S0579 MANIFLD/CANISTR PK -LF, REF DYNJ0259819I;  14) M1S0579 MANIFLD/CANISTR PK -LF, REF DYNJ0259819I;  15) M1S0579 MANIFLD/CANISTR PK -LF, REF DYNJ0259819I;  16) MINOR PACK-LF, REF DYNJ0410060S;  17) CYSTO I TRAY, REF DYNJ14063D;  18) CYSTO I TRAY, REF DYNJ14063D;  19) CYSTO PACK, REF DYNJ17310D;  20) DENTAL PK-LF, REF DYNJ21241D;  21) CYSTO PACK-LF, REF DYNJ25042I;  22) BASIC PACK-LF, REF DYNJ25450I;  23) BASIC PACK-LF, REF DYNJ25450J;  24) OPS 

## Reason for recall

XXX

## Distribution

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

## Key facts

- **Recall number:** Z-0166-2025
- **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-0166-2025

## Citation

> AI Analytics. FDA recall Z-0166-2025. Retrieved 2026-07-11 from https://api.ai-analytics.org/recall/Z-0166-2025. Source: US FDA. Licensed CC0.

---

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