FDA (Devices) recall action 82552
The FDA (Devices) publishes a recall like this one as 5 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 5 pages.
The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.
The agency’s own wording, quoted from the enforcement report.
The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.
Teleflex Medical is recalling 1,787 units of RUSCH LASERTUBE (Rubber) because the laser guard foil partially separated or detached at the edges.
Teleflex Medical is recalling 2,325 units of RUSCH LASERTUBE (Rubber) because the laser guard foil partially separated or detached at the edges.
Teleflex Medical is recalling RUSCH LASERTUBE devices because the laser guard foil may partially separate or detach at the edges.
Teleflex Medical is recalling RUSCH LASERTUBE devices because the laser guard foil partially separated or detached at the edges.
Teleflex Medical is recalling 4,312 units of RUSCH LASERTUBE (Rubber) because the laser guard foil partially separated or detached at the edges.