FDA DevicesClass II
Portex Spinal Tray, Item No. A3729-24 A3595
Published: January 21, 2026Recall ID: Z-1101-2026Category: devicesCountry: US
Reason for Recall / Hazard
Affected lots of syringes may have a crack on the syringe collar, which may lead to delayed or repeated blood draw/fluid delivery. This issue may also lead to blood leakage during sampling of arterial blood or leakage during fluid delivery.
Product Description & Identification
Portex Spinal Tray, Item No. A3729-24 A3595
Affected Products
Portex Spinal Tray, Item No. A3729-24 A3595
Additional Source Details
| Field | Value |
|---|---|
| City | Minneapolis |
| State | MN |
| Event id | 98168 |
| Address 1 | 6000 Nathan Ln N |
| Code info | 1. A3729-24 UDI-DI 30351688075691 Lots 6146204 (corrected on 1/22/26, removed "-LSM" suffix. 2. A3595 UDI-DI 35019517108211 Lot 6157980 |
| Postal code | 55442-1690 |
| Report date | 20260121 |
| Product type | Devices |
| Product quantity | 64290 total |
| Reason for recall | Affected lots of syringes may have a crack on the syringe collar, which may lead to delayed or repeated blood draw/fluid delivery. This issue may also lead to blood leakage during sampling of arterial blood or leakage during fluid delivery. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20251219 |
| Initial firm notification | Letter |
| Center classification date | 20260115 |
Overview
- Recalling FirmICU Medical Inc.
- StatusOngoing
- Risk LevelClass II
- DistributionUS Nationwide distribution in the states of CA, FL, IL, IN, MA, MI, MN, MO, NE, NJ, NY, OH, OK, TX, WA.