Olsen Medical recalls Symmetry bipolar forceps models with specific references due to potential seal compromise in sterile pouches. Affected units include various sizes and tip types.
Products may encroach into the sterile pouch seal thereby increasing the risk of the seal being compromised.
Olsen Medical is recalling specific models of Symmetry bipolar forceps because they may accidentally breach the sterile pouch seal. This could lead to contamination during medical procedures if the seal is compromised.
The forceps may encroach into the sterile pouch seal during use, which could cause the seal to become compromised. This might lead to contamination of the surgical site if the forceps are used without a properly sealed pouch.
Healthcare professionals using these forceps for surgical procedures are most at risk. Patients undergoing surgery with these instruments could face potential contamination if the seal is compromised.
Check for the product model names and reference numbers listed in the recall notice. Affected items include Symmetry Olsen bipolar forceps with specific sizes and tip types (e.g., 6.25" smooth 0.5mm tips, REF 20-0311).
Identify the reference number and quantity on the product packaging to confirm if it is affected.
The forceps may encroach into the sterile pouch seal, potentially compromising the seal and increasing the risk of contamination during medical procedures.
Check the reference number on the product packaging. Affected models include Symmetry Olsen bipolar forceps with specific sizes and tip types listed in the recall notice.
The recall does not specify a remedy, so contact Olsen Medical directly to confirm if your specific model is affected and what steps to take.
We’ve drafted a message you can send Olsen Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1944-2018 — Olsen Medical Olsen Medical Hello, I own a Olsen Medical that is covered by recall Z-1944-2018 from Olsen 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.
