CooperSurgical recalls LEEP Return Patient Pads with reversed expiration dates on outer boxes. This could lead to expired pads being used in procedures. Affected lots: 201809125 and 2: 201809135.
Discrepancy between the correct expiration dates on the individual pouches inside the boxes and incorrect expiration dates on the outer boxes, where the month and day were reversed.
CooperSurgical is recalling LEEP Return Patient Pads (10 per box) due to incorrect expiration dates on the outer boxes. The reversed month and day could cause expired pads to be used in procedures, potentially leading to ineffective treatment or safety issues.
The expiration dates on the outer boxes have the month and day reversed. This means the pads might expire before the procedure is completed, leading to ineffective treatment or potential safety risks.
Healthcare providers using CooperSurgical LEEP Return Patient Pads in electrosurgical procedures are most at risk. Patients receiving these pads may be affected if the pads expire during treatment.
Check the outer box for expiration dates labeled with the month and day reversed. Affected lots are 201809125 and 201809135.
Look for reversed month and day on the outer box expiration dates. Affected lots are 201809125 and 201809135.
The recall record states that the expiration dates on the outer boxes have the month and day reversed, but does not explain why.
Check the outer box for expiration dates labeled with the month and day reversed. Affected lots are 201809125 and 201809135.
The recall does not specify a remedy, so there is no action required beyond checking expiration dates.
We’ve drafted a message you can send CooperSurgical to request your refund or repair — edit it as you like.
Subject: Recall Z-2545-2019 — CooperSurgical CooperSurgical Hello, I own a CooperSurgical that is covered by recall Z-2545-2019 from CooperSurgical. 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.