Stradis Healthcare recalls curved tip syringes with item number 60060GCTS due to potential sterility breaches from incomplete bag sealing. Affected units include specific serial numbers and UDI codes.
Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.
Stradis Healthcare is recalling curved tip syringes that may have incomplete bag sealing, risking sterility breaches during medical procedures. This could lead to infections if used without proper sterility.
The syringes may have outer bags that aren't sealed properly during manufacturing. This could allow contamination, potentially causing infections if the sterile kit is used without proper sterility.
Healthcare professionals and patients using the recalled syringes for medical procedures. Those with specific serial numbers or UDI codes listed are most at risk.
Check for item number 60060GCTS on the syringe. Look for UDI codes M75260060GCTS1 (case) or M75260060GCTS0 (kit), and serial numbers starting with 22257490438.
Identify the item number, UDI codes, and serial numbers to confirm if your syringe is affected.
The recall is due to potential incomplete sealing of the outer bag, which could breach sterility and lead to infections during medical procedures.
Check for item number 60060GCTS, UDI codes M75260060GCTS1 (case) or M75260060GCTS0 (kit), and serial numbers starting with 22257490438.
The recall does not specify a remedy, so contact Stradis Healthcare directly for guidance.
We’ve drafted a message you can send Stradis Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0535-2023 — Stradis Healthcare Stradis Healthcare Hello, I own a Stradis Healthcare that is covered by recall Z-0535-2023 from Stradis Healthcare. 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.
