Complete FDA and NHTSA recall records dated in 2018, 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.
GE Healthcare has identified that some CT systems may have a damaged cable that can expose 120VAC to Service Engineers working inside the gantry.
The PPK System Spacer Block Alignment Tower mating feature that mates with the spacer block was undersized, which could potentially lead to mating issues between the devices. This could…
Philips has received several reports in which monitors with lithium ion batteries that had exceeded their battery life expectancy have overheated or ignited. These batteries should be…
Customer reports indicated an increase in the rate of non-detected MRSA in association with the VITEK 2 AST-P631 product.
There is a potential for an uncontrolled extension of iViewGT / XVI detector arms.
Packages labeled as containing 110mm rods may contain 100mm rods.
Two instrument holes located on the side of the plate, which act to align the saw guide are located on the wrong side of the plate
Philips has received several reports in which monitors with lithium ion batteries that had exceeded their battery life expectancy have overheated or ignited. These batteries should be…
Philips has received several reports in which monitors with lithium ion batteries that had exceeded their battery life expectancy have overheated or ignited. These batteries should be…
A cover failed leak testing during validation testing of new needle guides from a replacement tool.
Two lots of Genesis II Non Porous C/R Femoral Size 6 right packaged were distributed containing Genesis II C/R Femoral Size 4 left.
Product may be contaminated with Listeria monocytogenes.
Pasta Spinach with Cavatappi Reser's Fine Food is recalled due to a potential contamination with Cyclospora. The pasta salad contains spinach that was recalled due to a potential…
Roasted Chestnut loose leaf tea contains undeclared slivered almonds.
Product contains high levels of undeclared sulfites.
Sodium values reported on the product label are not consistent with the current value.
Potential blood contamination.
Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice Beverages due to packaging concerns following multiple reports of leaking caps.
Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice Beverages due to packaging concerns following multiple reports of leaking caps.
Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice Beverages due to packaging concerns following multiple reports of leaking caps.
HP Hood LLC, has initiated a recall of Blue Diamond Almond Breeze Almond Milk, Half Gallon, because the product tested positive for milk allergen.
Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice Beverages due to packaging concerns following multiple reports of leaking caps.
Sodium values reported on the product label are not consistent with the current value.
Product may be contaminated with Listeria monocytogenes.
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.
