Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
Caffeinated coffee was packaged in decaffeinated packaging.
IQF veggie Burger, and IQF Goat Tomato & Kale are being recalled due to potential Listeria monocytogenes or Salmonella contamination.
Buddy's Kitchen is recalling several products in response to the McCain Foods recall due to potential Listeria or Salmonella contamination.
60% Dark Chocolate Chips, bulk 30 lbs. containers, are recalled due to cross contamination with peanut.
Products recalled due to potential contamination with Listeria monocytogenes or Salmonella.
Product contains foreign material (plastic).
Individual pouches of Organic Minute Mug Cake Mix Celebration Confetti 4-pack do not declare milk as an allergen. The correct allergen statement is on the outer carton.
CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Lack of Assurance of Sterility
CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
General Motors LLC (GM) is recalling certain 2019 Buick Encore, Chevrolet Spark, Traverse, and Trax vehicles. The Sensing Diagnostic Module (SDM) on these vehicle may not have been turned…
Honda (American Honda Motor Co.) is recalling certain 2017-2019 Acura MDX, 2017-2018 Acura MDX Sport Hybrid, 2018-2019 Honda HR-V and Honda Odyssey, and 2016 Honda HR-V vehicles. The rear…
Convenience kits were sealed in immediate Tyvek pouches using incorrect specifications compromising product sterility
Users may experience alarm fatigue due to frequent alarming relating to patient temperature deviation beyond 0.5¿C while in Automatic mode. 2. Users may experience a Remove from Use code 9…
Coil overheating can occur when the device is used in Mode 2 setup. This could lead to a serious patient thermal injury. There have been no injuries reported as a result of this issue.
The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
Reprocessing instructions for the SGS/SGA Surgical Handpieces have been updated with instructions of manual cleaning and specific parameters for autoclave sterilization. The previous…
Convenience kits were sealed in immediate Tyvek pouches using incorrect specifications compromising product sterility
Browse recent months with enough recall history for useful comparison.
