BioPro recalls ceramic endoscopy heads with potential packaging defects that could compromise sterility, risking infection if implanted. Affected models include 13006-17296 series. No remedy specified.
Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.
BioPro is recalling ceramic endoscopy heads that may have packaging defects causing loss of sterility. If implanted, this could lead to infection. The recall covers specific model numbers and serial ranges.
The packaging defect could compromise the sterile barrier, meaning the device might not be sterile when implanted. This poses a potential infection risk if the device is used in surgery.
Patients scheduled for surgery using these specific ceramic endoscopy heads are most at risk. Medical professionals using the devices for procedures are also affected.
Check for model numbers 13006 through 17296 in the product list. All lots and serial numbers are affected. The devices are ceramic endoscopy heads used in surgical procedures.
Identify your device model number from the product list (e.g., 13006, 13012, etc.)
Reach out to BioPro, Inc. for further guidance on the recall
BioPro recalls these ceramic endoscopy heads due to a potential packaging defect that could compromise sterility, risking infection if implanted.
Affected models include 13006, 13012, 13013, 13019, 13007, 13008, 13009, 13010, 13011, 13014, 13015, 13016, 13017, 13018, 14823, 14824, 14825, 14826, and 17295, 17296.
The recall notice does not specify a remedy.
We’ve drafted a message you can send BioPro to request your refund or repair — edit it as you like.
Subject: Recall Z-0152-2026 — BioPro BioPro Hello, I own a BioPro that is covered by recall Z-0152-2026 from BioPro. 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.
