Complete FDA and NHTSA recall records dated in 2019, 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.
Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's Mochi six-piece products because of the potential for "free-floating" foreign plastic pieces in the product.
Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's Mochi six-piece products because of the potential for "free-floating" foreign plastic pieces in the product.
Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's Mochi six-piece products because of the potential for "free-floating" foreign plastic pieces in the product.
a limited number of Similac Pro-Advance 2oz. Ready to Feed (RTF) bottles from a single batch were packaged in Similac Pro-Sensitive cartons.
FDA sample tested positive for Listeria monocytogenes
Misbranding. Outer carton is incorrect and does not match labeling of yogurt tubes or product.
Product label declares Vitamin D3 at 200 IU per serving. FDA sample analysis revealed no Vitamin D in product.
Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's Mochi six-piece products because of the potential for "free-floating" foreign plastic pieces in the product.
Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's Mochi six-piece products because of the potential for "free-floating" foreign plastic pieces in the product.
Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's Mochi six-piece products because of the potential for "free-floating" foreign plastic pieces in the product.
Microbial Contamination of Non-Sterile Products: product failed bioburden testing for Total Aerobic Microbial Count.
Labeling: Incorrect or Missing Package Insert; an error in the Dosage Forms and Strengths section of the insert that incorrectly lists the tablet description coding for the tablets.
Lack of Assurance of Sterility
Subpotent Drug: Out of specification result during stability study in Pramipexole Dihydrochloride Tablets 0.125 mg
Subaru of America, Inc. (Subaru) is recalling certain 2020 Outback and Legacy vehicles. The brake pedal mounting bracket may have a missing or insufficiently tightened bolt.
Nissan North America, Inc. (Nissan) is recalling certain 2018-2019 Nissan Altima, Armada, Frontier, Kicks, Leaf, Maxima, Murano, NV, NV200, Pathfinder, Rogue, Rogue Sport, Sentra, Titan,…
The affected product is properly labelled with an expiration date of March 31, 2022; but the RFID programmed expiration date is April-2014 which results in an error message when connected…
Calibration; it has been determined that the capnographs may have been calibrated during manufacturing using a lower than specified concentration of CO2
Acetabular liners failed the oxidation testing performed prior to release. They may experience a higher wear rate, leading to revision surgery.
The manual does not provide instruction stating that exceeding 40 Celsius for extended periods can cause tissue damage.
Acetabular liners failed the oxidation testing performed prior to release. They may experience a higher wear rate, leading to revision surgery.
The manual does not provide instruction stating that exceeding 40 Celsius for extended periods can cause tissue damage.
A small crack at the box lock corner may after multiple cleaning and sterilization cycles produce an increased risk of corrosion, weakening the instrument and resulting in premature need…
software error in the central control unit of the floor stand.
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.
