Shippert Medical Technologies recalls Tissu-Trans FILTRON 1000 sterile medical devices due to unverified firm name on label. Affected units sold in specific zip codes in Colorado. Consumers should contact for remedy.
See the official notice for the full hazard description.
Shippert Medical Technologies is recalling Tissu-Trans FILTRON 1000 sterile medical devices because the firm name on the label may be incorrect. This could lead to improper use if the device is not properly identified by the correct manufacturer.
The hazard is not clearly described in the recall notice. The firm name on the label might be incorrect, which could lead to improper identification of the device. This might cause the device to be used incorrectly or not recognized as the intended medical product.
Patients using the Tissu-Trans FILTRON 1000 device for medical procedures in Colorado. Those with the device labeled with Shippert Medical Technologies in specific zip codes are most at risk.
Check the label for the firm name 'Shippert Medical Technologies' and the catalog number 3-TT-FILTRON 1000. The device is sold in specific zip codes in Colorado: 61627, 61687, 61839, 61920, 62051, and 62087.
Verify the firm name on the label is Shippert Medical Technologies and the catalog number 3-TT-FILTRON 1000.
The recall notice states the firm name on the label may be incorrect, but the hazard is not clearly described.
The affected zip codes in Colorado are 61627, 61687, 61839, 61920, 62051, and 62087.
Check the label for the firm name and catalog number. If it matches, contact Shippert Medical Technologies for further instructions.
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-1333-2019 — Shippert Medical Technologies Shippert Medical Technologies Hello, I own a Shippert Medical Technologies that is covered by recall Z-1333-2019 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
