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.
Positive bias in patient results at and below the cut-off of 60 U/mL with the lots listed in the table below when compared to alternate lots on the Atellica IM analyzer.
Devices from one lot of Perform" Reversed Inserts may contain a locking ring that was assembled upside down which would prevent the humeral insert from securely seating in the stem or…
If the DIVA touch display generates touch inputs without user interaction, due to possibility of the erroneous acknowledgement of a patient alarm, there is a potential for a delay in the…
Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity
Manual resuscitator circuit flow controller may come apart due to a missing manufacturing step.
The "DVOT brand" rapid test kits have not obtained the necessary authorization to be sold in the United States.
Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity
Blood leak sensor, a component of hemodialysis device, may show decreased sensitivity, at the lowest level, specified as 0.35 mL/min blood leak rate, which could delay triggering the…
Material with a quality issue was used in contact lens production, so contact lenses may not meet quality and/or performance standards for the entirety of their labeled shelf life, and…
The reason for this recall is Healgen Scientific Ltd. has determined that their Urinary Reagent Strip products have shown reduced sensitivity, or potential false negative results for the…
Updated labeling to ensure that blue cap on in-line valve is removed, prior to delivery of (Intrapulmonary percussive ventilation) IPV therapy.
Updated labeling to ensure that blue cap on in-line valve is removed, prior to delivery of (Intrapulmonary percussive ventilation) IPV therapy.
Insulin pumps that have been dropped, bumped, or experienced physical impact may have damage to internal electrical components, which may cause reduced pump battery life. Since the defect…
The bulk product used in the recalling firm's repackaged finished product was recalled due to bacterial contamination.
Required pasteurization temperatures were not achieved.
Undeclared whey (milk) & wheat flour; no nutrition fact panel & no contains statement
Undeclared wheat. The firm was notified by their supplier that they failed to include the allergen "wheat" on the label.
Undeclared whey (milk), wheat flour, almonds; no contains statement & no nutrition fact panel
Undeclared walnut and wheat. Mini Squash Harvest Loaf (UPC 8 55324 00505 3) was mis-labeled as Mini Raspberry Lemon Coffee Cake (UPC 8 57297 00745 4) and therefore wheat flour and walnuts…
Undeclared whey (milk), wheat flour, & bran (wheat); no nutrition fact panel & no contains statement
Undeclared whey (milk), wheat flour, & coconut; no nutrition fact panel & no contains statement
Eggs have the potential to be contaminated with Salmonella.
Potential foreign material (metal)
Acidified product was manufactured by firm without ODA license.
Browse recent months with enough recall history for useful comparison.
