Complete FDA and NHTSA recall records dated in April 2019.
These records include useful source details for the selected month.
The clear, plastic, polycarbonate hematocrit rotor may break apart during use and be ejected through the plastic housing, posing a safety hazard to the technician and potentially damaging…
Reports of pressure tubing separation between the sampling port and the high pressure tubing on certain lots of extravascular blood pressure transducers, which could lead to delay in…
Higher than anticipated occurrence of bone fracture during the use of the XR Tibia Posterior Punch
Upon servicing the gearwheel in the Emergency Drive the gearwheel may have been re-assembled incorrectly, leading to the inadequate operation of the Emergency Drive.
Potential lack of sterility assurance
The optional Vacuum Unit may stop working and display the failure message "Failure vacuum unit" during use.
The locking plate may be missing from the system, which may result in unexpected stand/table tilt movement that cannot be stopped by the user.
The locking plate may be missing from the system, which may result in unexpected stand/table tilt movement that cannot be stopped by the user.
The product does not meet sterility requirements. Product labeled as sterile was distributed without undergoing sterilization prior to distribution.
The clear, plastic, polycarbonate hematocrit rotor may break apart during use and be ejected through the plastic housing, posing a safety hazard to the technician and potentially damaging…
The Integrated ECG cable with 3-lead leadwires can short circuit during defibrillation and conduct 25% of the defibrillation energy away from the patient.
Reports of pressure tubing separation between the sampling port and the high pressure tubing on certain lots of extravascular blood pressure transducers, which could lead to delay in…
Paltop Surgical Kits contain 1.25mm Hex Driver(s) which may have a slightly oversized hex driving feature, make it difficult to engage screws and abutments containing the corresponding…
Reports of pressure tubing separation between the sampling port and the high pressure tubing on certain lots of extravascular blood pressure transducers, which could lead to delay in…
Higher than anticipated occurrence of bone fracture during the use of the XR Tibia Posterior Punch
The locking plate may be missing from the system, which may result in unexpected stand/table tilt movement that cannot be stopped by the user.
The locking plate may be missing from the system, which may result in unexpected stand/table tilt movement that cannot be stopped by the user.
The product was designed for 120V usage and is being used in South Africa with 220V. There is a potential for the device to overheat and the mouthpiece can pop off.
The firm issued an updated instructions for use to reduce the potential for phrenic nerve injury.
Higher than anticipated occurrence of bone fracture during the use of the XR Tibia Posterior Punch
The clear, plastic, polycarbonate hematocrit rotor may break apart during use and be ejected through the plastic housing, posing a safety hazard to the technician and potentially damaging…
Paltop Surgical Kits contain 1.25mm Hex Driver(s) which may have a slightly oversized hex driving feature, make it difficult to engage screws and abutments containing the corresponding…
Soom Foods is recalling its 1oz Chocolate Sweet Tahini Halva Spread squeeze packs (Code: 67333D)because our contracted manufacturer, Xela Pack, discovered Salmonella in a sample.
The ingredients statement declared wheat, soybean oil, soy lecithin, eggs, and milk. The Contains statement does not declare milk.
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.
