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 firm received positive test results for Listeria monocytogenes in a product that was housed in the same storage bin.
Product has the potential to be contaminated with Listeria monocytogenes.
The firm received positive test results for Listeria monocytogenes in a product that was housed in the same storage bin.
Product has the potential to be contaminated with Listeria monocytogenes.
Ziyad Brothers Importing is voluntarily recalling its Ziyad Brand Tahini, 8 oz. 16 oz., 1/2 gallon and 32 oz. sizes due to potential contamination with Salmonella.
Product has the potential to be contaminated with Listeria monocytogenes.
The firm received positive test results for Listeria monocytogenes in a product that was housed in the same storage bin.
The firm received positive test results for Listeria monocytogenes in a product that was housed in the same storage bin.
The firm received positive test results for Listeria monocytogenes in a product that was housed in the same storage bin.
Marketed Without An Approved NDA/ANDA: FDA analysis found products to contain undeclared sildenafil and tadalafil. The presence of sildenafil and tadalafil makes these products an…
Marketed Without An Approved NDA/ANDA: FDA analysis found products to contain undeclared sildenafil and tadalafil. The presence of sildenafil and tadalafil makes these products an…
BMW of North America, LLC (BMW) is recalling certain 2018-2019 BMW X3 xDrive30i, X3 sDrive30i, and X3 M40i vehicles equipped with the "Active Lane Keeping Assistant" option. The steering…
The products exhibit an unpleasant odor due to microbial contamination with Yarrowia lipolytica.
Firm is notifying customers that the Deep-Cleaning Service is now available in the United States. Stockert Heater-Cooler System 3T devices are suspected of microbial contamination and may…
The affected products were inadvertently packaged with the inner packaging pouch being sealed together with the outer pouch.
Specific lots of EXACTAMIX Inlets listed below due to incorrectly performed over-labeling. The inlets were over-labeled with a blank label, or with a label containing an extended expiration…
Getinge has received complaints concerning the X TEN Surgical Lights whose spring arms have broken, causing light heads to separate from the assembly. The issue relates to cracking of the…
Specific lots of EXACTAMIX Inlets listed below due to incorrectly performed over-labeling. The inlets were over-labeled with a blank label, or with a label containing an extended expiration…
A single lot of GENESIS II FEMORAL FIVE DEGREE VALGUS BUSHING due to a laser mark labeling error. The left valgus bushing was incorrectly laser marked as right and vice versa.
Specific lots of EXACTAMIX Inlets listed below due to incorrectly performed over-labeling. The inlets were over-labeled with a blank label, or with a label containing an extended expiration…
The affected products were inadvertently packaged with the inner packaging pouch being sealed together with the outer pouch.
The Strip Provider Modules (SPM) on some of the instruments had not been inspected during manufacture for correct seal placement and integrity.
The products exhibit an unpleasant odor due to microbial contamination with Yarrowia lipolytica.
Possible leak at distal open end of the strain relief, which causes medical staff to continue adding inflation fluid to maintain balloon pressure for adequate occlusion of the ascending…
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