Teleflex Medical recalls specific RUSCH LASERTUBE rubber products due to potential laser guard foil detachment. Affected units have specific lot numbers and sizes. No remedy provided in recall notice.
The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.
Teleflex Medical is recalling certain RUSCH LASERTUBE rubber products because the laser guard foil may partially separate or detach at the edges. This could lead to unintended laser exposure during medical procedures.
The laser guard foil in these products can partially separate or detach at the edges. This may allow unintended laser exposure to the user or patient during medical procedures, potentially causing injury.
Medical professionals using the RUSCH LASERTUBE rubber products with specific lot numbers and sizes are likely affected. Patients using these devices may be at risk if the laser guard foil detaches during procedures.
Check for the product name 'RUSCH LASERTUBE (Rubber)', order number 102004-000070, reference number 102004, and size ID 7.0 mm. Affected units have specific lot numbers listed in the recall notice.
Identify the product name, order number, reference number, and size ID to confirm if your unit is affected.
The recall notice does not provide a remedy for this issue.
The recall notice does not specify any action steps for affected units.
Check the product name 'RUSCH LASERTUBE (Rubber)', order number 102004-000070, reference number 102004, and size ID 7.0 mm. Affected units have specific lot numbers listed in the recall notice.
We’ve drafted a message you can send Teleflex Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1685-2019 — Teleflex Medical Teleflex Medical Hello, I own a Teleflex Medical that is covered by recall Z-1685-2019 from Teleflex 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.
