Complete FDA and NHTSA recall records dated in 2023, 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.
In the event of any unintended table movement, the system may not detect the incorrect direction, could lead to the injury of a patient, staff member, operator, or equipment.
The incorrect IFU was distributed with the devices.
Rakkyo was removed because the firm provided the updated ingredients statement to consignees. Product does not contain any allergens.
Water bottle has a cup with a screw cap attached by a weld that has been found to leach lead.
Seasoned Garlic with Salt and Vinegar was removed because the firm provided the updated ingredients statement to consignees. Product does not contain any allergens.
Cucumber Pickle was removed because the firm provided the updated ingredients statement to consignees. Product does not contain any allergens.
Seasoned Perilla Leaves was recalled due to undeclared Sesame Seeds, Soybean, Wheat, Fish (Anchovy), and Shrimp.
Perilla Leaves in Soybean Paste was recalled due to undeclared Soybean, Wheat, Fish (Anchovy, Big Eye Herring), and Shrimp.
Peanuts are declared in the ingredients statement, but they are not declared in the allergen contains statement.
Xin Ao International Group Corp, 601 E. Linden Ave Linden NJ 07036is initiating a recall of Enoki Mushroom, 200g, Plastic Bag, 25 bags per case because the product may be contaminated with…
The firm's vanilla product contains coumarin, a prohibited substance.
Seasoned Radish Sliced was recalled due to undeclared Fish (Anchovy, Big Eye Herring), Crustacean (Shrimp), Sesame.
Seasoned Fish Meat was recalled due to undeclared Fish (Pollock, Golden Threadfin Bream, Hairtail, Lizard Fish), Wheat, and Soy bean.
Stir-Fried Fish Cake was recalled due to undeclared Soybean, Wheat, Fish (Golden Threadfin Bream, Hairtail), and Sesame.
undeclared soy proteins
CGMP Deviations: Detection of N-nitroso-dabigatran (NDAB) impurity levels above the Acceptable Daily Intake Limit.
Lack of assurance of sterility: Suspected microbial growth present on external label packaging.
CGMP Deviations: Detection of N-nitroso-dabigatran (NDAB) impurity levels above the Acceptable Daily Intake Limit.
Failed Impurities/Degradation Specifications and Subpotent Drug: High Out of Specification results for a known and unknown impurity as well as low Out of Specification results for assay.
Tesla, Inc. (Tesla) is recalling certain 2023 Model X vehicles equipped with a full self-driving computer 4.0 and running software release version 2023.2.200. Weak camera signal strength…
Tesla, Inc. (Tesla) is recalling certain 2018-2019 Model 3 vehicles. The front suspension lateral link fasteners may loosen, allowing the lateral link to separate from the sub-frame.
Automated dispensing cabinet drawer firmware may have inadvertently been downgraded to an earlier version of drawer firmware during new device installations or device replacement upgrades,…
The subject product lots are being recalled because they received a higher than specified irradiation dose. This exceeds the validated range for exposure to gamma radiation of these devices…
There have been reports of excessive condensation associated with certain lots of the Low Flow Disposable Patient Circuits (DPCs) used with Precision Flow System which may lead to excessive…
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.
