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.
Retention of Outdated Information in an Order Set. In the Care Plan Library, double clicking to add or delete a Component/Procedure to an Order Set does not trigger the update of the…
The Access immunoassays are susceptible to biotin interference.
The device collar size was incorrectly labeled as 25 mm where it should be recorded as 32 mm
Cracks may occur over time on the tube holding shaft near the base of the tube mounting flange.
The firm determined that the labeling (surgical technique) should be updated to clarify the proper technique and instrumentation to perform calcar planing to the bone, i.e., to include a…
It was discovered that one Ranger Pressure lnfusor Model 145, SN: 100873, produced a left chamber pressure that was slightly below the manufacturing specification.
A customer experienced when using IMPAX CV Reporting software, specifically, when building a NIV report, the NIV Cardio report was showing incorrect findings for Aneurysm.
Mindray has received two reports from outside the United States that the battery pack for TI transport monitor/module overheated.
Lack of sterility assurance. There is a defect in the primary packaging of the device, which may compromise the device sterility
The Access immunoassays are susceptible to biotin interference.
Individual vials of calibrator and standard were mislabeled; specifically the units on the vial labels are incorrectly listed as mg/dl when the correct unit is mg/L.
The device collar size was incorrectly labeled as 25 mm where it should be recorded as 32 mm
da Vinci Xi(R) Surgical System Patient Side Carts (PSC) were shipped to the field with potentially under-torqued brake screws in a section of the system arms.
Cracks may occur over time on the tube holding shaft near the base of the tube mounting flange.
FANA200 kit lot TS 3577 was re-worked due to shortened shelf-life. The alert sticker on the kit box of the lot informed customers that the shelf-life had been shortened and referenced a…
Under certain conditions, the cables used with the Hemo system during a patient procedure could stop displaying the patient SpO2 causing a slight delay in patient care.
ROTH MOBELI grab handles could detach and patient could fall if the EOS system operator does not follow instructions. Before each use, the operator must examine the vacuum safety indicator…
Under certain conditions, the cables used with the Hemo system during a patient procedure could stop displaying the patient SpO2 causing a slight delay in patient care.
The device collar size was incorrectly labeled as 25 mm where it should be recorded as 32 mm
The firm was notified that the product does not list MILK in the allergen Contains statement, although it is listed in the ingredient statement. They were alerted of this error by a…
Firm is recalling a limited number of Green Tea and Red Bean ice cream due the possibility of the presence of metal fragments.
Firm is recalling a limited number of Green Tea and Red Bean ice cream due the possibility of the presence of metal fragments.
The firm was notified by a customer that the label does not include Pecans or Tree Nuts in the Allergy contain statement.
Product contains undeclared tree nuts-cashews
Browse recent months with enough recall history for useful comparison.
