Boston Scientific recalls PFR Kit Pinnacle Anterior Apical model M0068317100 for pelvic organ prolapse treatment. No specific hazard or remedy details provided in official recall.
See the official notice for the full hazard description.
Boston Scientific is recalling a specific PFR Kit for pelvic organ prolapse repair. The recall does not state a hazard or remedy, so no action is needed based on this notice.
The recall does not describe any hazard or risk to users. No safety concerns are mentioned in the official notice.
Women who have received this PFR Kit for pelvic organ prolapse repair are likely affected. The recall does not specify who is at higher risk.
This kit has model number M0068317100 and batch number ML00002841. It was sold with GTIN 08714729773047 for pelvic organ prolapse treatment.
Look for model number M0068317100 and batch number ML00002841 on the kit.
The official recall notice does not state a hazard or reason for recall.
No action is required as the recall does not specify a hazard or remedy.
Check for model number M0068317100 and batch number ML00002841.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-1624-2018 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-1624-2018 from Boston Scientific. 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.
