Complete FDA and NHTSA recall records dated in 2019, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
The anti-tip tubes potentially fail in certain situations and the wheelchairs can tip backwards.
The action has been initiated to address reports of burst balloons which have resulted in significant difficulty retrieving the device into the sheath and withdrawing the system from the…
False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
Mislabeling - Some unit of sale packages (bags of 100 sets of MPC-125) were found to be incorrectly labeled as Molded Products Male to Male Luer Adapters, Catalog # MPC-150.
Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Outflow Graft leaking at the pump connection during the implantation process. If the C-Ring is insufficiently seated, it renders the device nonfunctional because the Outflow Graft…
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
The action is being initiated due to internal testing which identified a possibility for transducers to exceed the acoustic output power (AOP) values defined . The transit voltage values…
The action is being initiated due to internal testing which identified a possibility for transducers to exceed the acoustic output power (AOP) values defined . The transit voltage values…
False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
An incorrect control board and firmware installed in some of the Hand Held Barcode Scanners could result in sample/patient mismatch or duplicate results (from other patients specimens) for…
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
The action is being initiated due to internal testing which identified a possibility for transducers to exceed the acoustic output power (AOP) values defined . The transit voltage values…
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Visual particulates within a battery Tyvek pouch. The battery is provided sterile for use with surgical drivers.
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
The action has been initiated to address reports of burst balloons which have resulted in significant difficulty retrieving the device into the sheath and withdrawing the system from the…
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.
