# FDA recall Z-1724-2026

> **Medline Industries, LP** · Class I · device recall initiated 2026-02-27.

## Product

Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows:    1. MTS RH LFT HRT KIT, Medline SKU # 60010508;   2. MTS 3V W/GUIDE, Medline SKU # 60100701;   3. ANGIOGRAPHY KIT, Medline SKU # 60131209;   4. MTS LHK, Medline SKU # 60160075;   5. MTS LHK, Medline SKU # 60161954;   6. MTO LHK, Medline SKU # 60230148;   7. GENERAL SURGERY TRAY, Medline SKU # 00-500510I;   8. BIOBURDEN TEST KIT - 686, Medline SKU # BIOB686;   9. RADIO ANGIO UNIV HOSP PACK-LF, Medline SKU # DYNJ0376145M;   10. SPECIALS PACK-LF, Medline SKU # DYNJ0392706K;   11. CARDIAC CATH PACK-LF, Medline SKU # DYNJ0451426O;   12. CARDIAC CATH PACK-LF, Medline SKU # DYNJ0451426P;   13. CARDIAC CATH PACK, Medline SKU # DYNJ07953N;   14. CATH PACK-LF, Medline SKU # DYNJ0803367J;   15. E.P. TRAY, Medline SKU # DYNJ19343J;   16. CARDIAC CATH PACK, Medline SKU # DYNJ20898T;   17. CATH LAB TRAY, Medline SKU # DYNJ24250G;   18. CATH LAB PACK-LF, Me

## Reason for recall

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

## Distribution

Worldwide distribution: US (nationwide) including Puerto Rico (PR) and OUS (foreign) to countries of: Canada (CA), Netherlands (NL), Australia (AU), Korea, Republic of (KR), Sri Lanka (LK), Pakistan (PK), Japan (JP), United Arab Emirates (AE), Singapore (SG) and Slovakia (SK).

## Key facts

- **Recall number:** Z-1724-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-02-27
- **Report date:** 2026-04-15

- **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-1724-2026

## Citation

> AI Analytics. FDA recall Z-1724-2026. Retrieved 2026-08-12 from https://api.ai-analytics.org/recall/Z-1724-2026. Source: US FDA. Licensed CC0.

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