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All product recalls associated with Teleflex Medical.
Total Recalls
1000
Past Year
1000
Class I (Serious)
34
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Mislabeling-The rebreathing bag is incorrectly labeled as a 1 liter bag when it is actually a 1/2 liter bag.
The recall involves Weil-McLain Ultra 80, Ultra 105, Ultra 155, Ultra 230 and Ultra 310 condensing, high-efficient, gas-fired boilers for space heating. The user's manual and installation manual have "Ultra Gas-Fired Water Boiler" on the cover. The boilers are wrapped in a glossy silver/flat black jacket and either stand on the floor or are wall-mounted. The serial numbers range from CP5071716 through CP5327000. When the panel on the front of the boiler is removed, a bar-coded label with the serial number is located on the lower right hand side of the boiler itself. "Weil-McLain" is written on the front panel of the boilers.
Misbranded: Tray label states 26G x 5/8 inch, needle is 25 G x 1 inch
AC inlet connector failure that can result in thermal damage to the humidifier enclosure and/or ignition of materials external to the device
AC inlet connector failure that can result in thermal damage to the humidifier enclosure and/or ignition of materials external to the device
The recalled kits include plastic ears, eyes, noses, mouth, hands, shoes, hats, eyeglasses and jewelry that are used to decorate Halloween pumpkins. The recall includes Mr. Potato Head "Make a Monster Pumpkin" and "Make a Fireman Pumpkin" and Mrs. Potato Head "Make a Diva Pumpkin." The products are labeled for ages 2 and older. Products with small parts intended for children under 3 years old are prohibited due to a choking hazard.
These lithium-ion batteries were sold with, or sold separately to be used with, the following notebook computer models: Computer Manufacturer Computer Model Battery Model Fujitsu LifeBook: P1510, P1510D, P7120, P7120D, S7020, S7020D, C1320D, Q2010, T4210 CP229720-01, CP229725-01, CP234003-01, CP234019-01, CP255100-01, CP255108-01, CP267910-01, CP267915-01, CP283030-01, CP293420-01 Gateway Gateway: CX200, CX210, E100M, M250, M255, M280, M285, M465, M685, MP8708, NX260, NX510, NX560, NX860, NX100, MX1025, MX6918b, and MX1020j 916C4610F, 916C4720F, 916C4730F, 916C5010F, W230 Sony Sony VAIO: VGN-FE550G, VGN-FE570G, VGN-T240P, VGN-T250, VGN-T250P, VGN-T260P, VGN-T270P, VGN-T340P, VGN-T350, VGN-T350P, VGN-T360P, VGN-T370P VGP-BPS3A, VGP-BPS2B Toshiba Portege: M300, M400/M405, S100/S105 Qosmio: G35 Satellite: R10/R15 Tecra: A2, M3, M4, M5, M6, and S3 PA3191U-4BRS, PA3356U-2BRS, PA3475U-1BRS, PA3191U-5BRS, PA3356U-3BRS, PA3476U-1BRS The battery model can be found on the battery's label.
Metal bone fragmentor was causing metal shavings to be released into the resultant fragmented tissue during use.
Counterfeit-blood glucose test strips (manufacturer unknown)
Erroneous Test Results: Monitor may display 'error' message or report falsely elevated patient results caused by insufficient amounts of active ingredient (thromboplastin) in the test strips.
Fibrin Analysis Catheter Testying System contains the ''Luer Lok Access Device'' that fails to lock securely to certain catheter devices because the male luer taper surface is not within the specification of the taper.
Loose fixation pegs: One lot of femoral components may have loose fixation pegs.
During programming, pulse generator may be inadvertently set to 8.0 mA output, regardless of the mA range selected by the clinician
During programming, pulse generator may be inadvertently set to 8.0 mA output, regardless of the mA range selected by the clinician
Counterfeit Glucose Test Strips (manufacturer unknown)
Incorrect expiration date: The product's exterior box date may be labeled with a longer than actual expiration date (the pouch label is correct)
Counterfeit Glucose Test Strips (manufacturer unknown)
Possible excessive RF exposure/may burn
There have been reports of difficulty separating the Gambro Cartridge Blood Set from Asahi Reuse/Multiple Use Dialyzers at the end of treatment, possibly damaging the dialyzer nozzle.
There have been reports of difficulty separating the Gambro Cartridge Blood Set from Asahi Reuse/Multiple Use Dialyzers at the end of treatment, possibly damaging the dialyzer nozzle.