Glazed ceramic plates are recalled because they may exceed FDA guidance levels for leachable lead (3.0mg/L).
All Recalls
95,114 total recalls in our database
🍎 Food Class I - Dangerous
Undeclared peanuts
Signature Blue Swimming Crab Claw and Lump 1lb can Tin Can, Lot # 78821 Expiration June 09th 2026, Lot # 788454 Expiration June 09th 2026
Pacific Shellfish
🍎 Food Class I - Dangerous
Product was recalled due to the temperature being over 40 degrees and not on ice July 1st, 2024
Potential undeclared gluten product is labeled as gluten free but consumer advocacy group testing revealed results above 20ppm for gluten.
Complete 30C/200C Homeopathic Kit, Contains: One hundred 1/2 dram vials of homeopathic medicines, Washington Homeopathic Products, Inc., Berkley Springs, WV 25411, UPC 7 40640 64300 6.
Washington Homeopathic Products
💊 Drugs Class I - Dangerous
Labeling: Label Mix-up: Some bottles of Ferrum Phosphoricum 200C were incorrectly labeled as Ferrum Metallicum 200C.
💊 Drugs Class I - Dangerous
Failed Dissolution Specifications: Out-of-specification results observed for dissolution testing at the 8-hour and 12-hour pull intervals.
💊 Drugs Class I - Dangerous
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
💊 Drugs Class I - Dangerous
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
💊 Drugs Class I - Dangerous
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
💊 Drugs Class I - Dangerous
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
🏥 Medical Devices Class I - Dangerous
Issue with analyzer when the pH of the calibration solution decreases during the in-use period potentially because of bacterial growth in the calibration solution bottles. This may result in a probability of reporting biased out-of-specification pH results on blood samples.
🏥 Medical Devices Class I - Dangerous
The LinkSymphoKnee Patella Sizing Template was incorrectly labeled. The markings on two arms of the instrument were mixed up because the triangular Patella Sizing Template was inserted upside down into the laser marking process.
🏥 Medical Devices Class I - Dangerous
Perfusor Space Syringe Pump's instructions for use previously identified Monoject syringes as an option for use. However, changes to manufacturing to Cardinal Health Monoject syringes may result in issues with recognition, compatibility, and pump performance, such as overdose, underdose, delay in therapy, delay in occlusion alarms, and delay in feeding. Cardinal Health Monoject syringes are not compatible with the indicated pumps.
🏥 Medical Devices Class I - Dangerous
Their is a potential that the implantable pulse generator replacement indicator and end of service date may be shorter than indicated in the product labeling potentially resulting in loss of therapy.
The IFU was missing some risk information requested by another country to be contained in the IFU pertaining to potential complications.
🏥 Medical Devices Class I - Dangerous
Their is a potential that the implantable pulse generator replacement indicator and end of service date may be shorter than indicated in the product labeling potentially resulting in loss of therapy.
TourniKwik Tourniquet Set (CFN 79012)
Medtronic Perfusion Systems
🏥 Medical Devices Class I - Dangerous
Incorrect component placed in four manufactured lots of the TourniKwik" Tourniquet Set.
🏥 Medical Devices Class I - Dangerous
If the Sensis documentation functionality is used during adding of once-per-study reporting events (e.g., Type 1 events, as further defined in the administrator manual), the possibility exists that the application could crash.
🏥 Medical Devices Class I - Dangerous
Perfusor Space Syringe Pump's instructions for use previously identified Monoject syringes as an option for use. However, changes to manufacturing to Cardinal Health Monoject syringes may result in issues with recognition, compatibility, and pump performance, such as overdose, underdose, delay in therapy, delay in occlusion alarms, and delay in feeding. Cardinal Health Monoject syringes are not compatible with the indicated pumps.
🏥 Medical Devices Class I - Dangerous
Perfusor Space Syringe Pump's instructions for use previously identified Monoject syringes as an option for use. However, changes to manufacturing to Cardinal Health Monoject syringes may result in issues with recognition, compatibility, and pump performance, such as overdose, underdose, delay in therapy, delay in occlusion alarms, and delay in feeding. Cardinal Health Monoject syringes are not compatible with the indicated pumps.