ICU Medical recalls Portex Spinal Tray models A3729-24 and A3595 due to potential cracks in syringe collars causing blood leakage or repeated blood draws. Affected units include specific lots with UDI-DI numbers.
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.
ICU Medical is recalling Portex Spinal Trays with model numbers A372:24 and A3595 because some units may have cracks in the syringe collar. This can cause blood leakage during blood sampling or repeated blood draws, which might lead to inaccurate results or discomfort.
Cracks in the syringe collar can cause blood to leak during arterial blood sampling or fluid delivery. This may result in repeated blood draws or inaccurate test results, but does not typically cause serious injury.
Healthcare professionals using these spinal trays for blood sampling or fluid delivery are most at risk. Patients receiving blood tests or fluid treatments with affected units could experience leakage or repeated draws.
Check for Portex Spinal Trays with model numbers A3729-24 or A3595. Affected units have specific UDI-DI numbers: 30351688075691 for lot 6146204 and 35019517108211 for lot 6157980.
Inspect the syringe collar for cracks before use. If present, stop using the tray immediately.
The recall is due to potential cracks in the syringe collar of affected Portex Spinal Trays, which may cause blood leakage or repeated blood draws.
Model numbers A3729-24 and A3595 with specific UDI-DI numbers 30351688075691 and 35019517108211 are affected.
Check the UDI-DI number on the tray. Affected units include lot 6146204 (UDI-DI 30351688075691) and lot 6157980 (UDI-DI 35019517108211).
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1101-2026 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-1101-2026 from ICU Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
