Kirwan Surgical Products recalls Ambler Surgical Bipolar Pencil 25 Gauge Straight (model PD7226) due to potential outer steel tube breaking or detaching during eye surgery. This could cause injury to patients or surgeons.
Potential for the outer stainless-steel tube to break or detach.
Kirwan Surgical Products is recalling Ambler Surgical Bipolar Pencil 25 Gauge Straight (model PD7226) because the outer stainless-steel tube might break or detach during surgery. This poses a risk of injury to patients or surgeons if the tube separates unexpectedly.
The outer stainless-steel tube could break or detach during surgical procedures, especially when used for delicate eye surgeries. This might cause the pencil to become unstable or injure the patient or surgeon if the tube separates unexpectedly.
Surgical teams and hospitals using the Ambler Surgical Bipolar Pencil 25 Gauge Straight (model PD7226) for eye or soft tissue procedures are affected. Surgeons and patients at risk during procedures using this specific product.
Check for the model number PD7226 on the product packaging. The product was sold with expiration dates from September 1, 2027, onward.
Verify the model number on the packaging to confirm if it's PD7226.
Reach out to Kirwan Surgical Products for guidance on next steps if you have the recalled product.
The outer stainless-steel tube could break or detach during eye surgery, potentially causing injury to patients or surgeons.
The model number is PD7226.
Check for the model number PD7226 on the packaging, and the product was sold with expiration dates from September 1, 2027, onward.
We’ve drafted a message you can send Kirwan Surgical Products to request your refund or repair — edit it as you like.
Subject: Recall Z-0657-2025 — Kirwan Surgical Products Kirwan Surgical Products Hello, I own a Kirwan Surgical Products that is covered by recall Z-0657-2025 from Kirwan Surgical Products. 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.
