Valeris Medical recalls Apollo Medial Suture Anchor (MSA-4515) due to mislabeling with incorrect suture type. Affected units contain 5 packages per container, sterile, Rx only.
The product was mislabeled as containing the incorrect type of suture.
Valeris Medical is recalling its Apollo Medial Suture Anchor (catalog number MSA-4515) because it was mislabeled with the wrong suture type. This could lead to improper medical use if the incorrect suture is used during surgery.
The product was mislabeled as containing the incorrect type of suture. This means the suture might not be suitable for the intended surgical procedure, potentially causing complications during surgery.
Medical professionals who have purchased this suture anchor for surgical use are likely affected. Patients receiving this product during surgery may be at risk if the incorrect suture is used.
Check for the catalog number MSA-4515 on the product label. The package contains 5 sterile suture anchors per container, with a lot number of 1982 and expiration date 3/22/2019.
Look for the catalog number MSA-4515 and lot number 1982 on the product label.
The product was mislabeled with the incorrect suture type, so it may not be suitable for surgical use. Consult your healthcare provider for guidance.
The official recall notice does not specify a remedy for this product. Check the product label for the catalog number MSA-4515 and lot number 1982.
The product contains 5 sterile suture anchors per container with a lot number of 1982 and expiration date 3/22/2019.
We’ve drafted a message you can send Valeris Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0104-2019 — Valeris Medical Valeris Medical Hello, I own a Valeris Medical that is covered by recall Z-0104-2019 from Valeris Medical. 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.
