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.
The item is being recalled due to an inadequate pouch seal. This defect has the potential to lead to a loss of sterile pouch integrity, which could impact the products sterility assurance…
The torque wrench used to tighten system bolts during installation was found to be out of tolerance
It was reported that an implant labeled as 343-13-708 was packaged with implant 343-19-707.
Product is labeled to be caffeine-free but contains caffeine.
Product contains undeclared coconut.
Product contains undeclared eggs and soy.
Milk is not declared on the product labeling.
General Mills is recalling 2 production runs of Cascadian Farm Organic Cinnamon Raisin Granola due to undeclared nut allergen, almond.
Thanlwin Fried Bean Snack is being recalled due to undeclared peanuts.
The firm is recalling their Store Made BLT sandwich due to undeclared egg found in the mayonnaise ingredient. The firm received an illness complaint reporting that egg was not declared in…
Product is recalled due to potential under processing.
Failed Impurities/Degradation Specifications: manufacturer of product recalled this repackaged lot due to out of specification results for related compound.
Temperature Abuse: Prolonged exposure to temperatures outside of labeled storage conditions.
Failed Stability Specifications
Temperature Abuse: A portion of this product lot was exposed to subfreezing temperatures, which is outside of the acceptable storage range listed on the product labeling, during transit to…
Labeling; Label Mixup; the immediate package is labeled incorrectly as Chloroprep Onestep (Clear), however, the correct label should be Chloroprep with Tint (Hi Lite Orange)
Failed Impurities/Degradation Specifications: 5mg strength being recalled for out of specification results for related compound.
Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making this an…
Cross contamination with other products: traces of Dapsone were found in the finished product.
The VCLAS 3mm, 10mm, and 15mm tip devices were not appropriately tested for saline leakage during the manufacturing process.
Customers have reported a higher than expected number of invalid test results when using the recalled product per the package insert.
New pacemaker firmware was developed to further mitigate the risk of unauthorized access to our pacemakers that utilize radio frequency (RF) communications.
New pacemaker firmware was developed to further mitigate the risk of unauthorized access to our pacemakers that utilize radio frequency (RF) communications.
During a bolus tracking procedure, no images were generated when the scan was completed, and the raw data file was not available for offline reconstruction. There is a discrepancy between…
Browse recent months with enough recall history for useful comparison.
