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 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.
Product contains undeclared milk.
Risk of Hepatitis A exposure.
The ingredients statement declared wheat, soybean oil, eggs, soy lecithin, and WHEY. The ingredients statement does not declare Milk as a source of whey and the Contains statement does not…
The ingredients statement declared wheat, milk, eggs, pecan and peanut oil. The Contains statement does not declare peanut oil.
Mis-packaging; product is labeled as Reduce L-Glutathione but actually contains Lithium Orotate.
The ingredients statement declared wheat, soybean oil, eggs, soy flour, soybean oil, and WHEY. The ingredients statement does not declare Milk as a source of whey and the Contains statement…
The ingredients statement declared wheat, soybean oil, eggs, soy flour, soybean oil, and WHEY. The ingredients statement does not declare Milk as a source of whey and the Contains statement…
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.
