Shippert Medical Technologies recalls Tissu-Trans Syringe Fill 360 syringes due to potential pouch cuts or holes that could compromise sterility. Affected units have the catalog number 3-TT-SFILL 360.
The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch.
Shippert Medical Technologies is recalling Tissu-Trans Syringe Fill 360 syringes because the pouch might have cuts or holes that could allow contamination. This poses a risk of infection if the syringe is used without proper visual inspection.
The syringe pouch may contain hidden cuts or holes that aren't visible to the naked eye. If the pouch is compromised, the sterile contents could become contaminated during use, increasing infection risk.
Healthcare professionals and patients who use the Tissu-Trans Syringe Fill 360 syringes for medical injections. Those most at risk are individuals who rely on the syringe for sterile procedures without checking the pouch for damage.
Check for the catalog number 3-TT-SFILL 360 on the syringe label. The manufacturer name on the label is Shippert Medical Technologies, Centennial, CO.
Inspect the syringe pouch for any visible cuts or holes before use.
The syringe may have hidden cuts or holes that could compromise sterility, so it's not safe to use without visual inspection.
Look for the catalog number 3-TT-SFILL 360 on the syringe label, with the manufacturer name Shippert Medical Technologies.
The recall does not specify a remedy, so check the pouch for damage before use. If damaged, do not use the syringe.
We’ve drafted a message you can send Shippert Medical Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-1336-2019 — Shippert Medical Technologies Shippert Medical Technologies Hello, I own a Shippert Medical Technologies that is covered by recall Z-1336-2019 from Shippert Medical Technologies. 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.
