Complete FDA and NHTSA recall records dated in October 2021.
These records include useful source details for the selected month.
Tesla, Inc. (Tesla) is recalling certain 2017-2021 Model S, Model 3, Model X, and 2020-2021 Model Y vehicles operating software version 2021.36.5.2. A communication error may cause false…
Labeled On-board instrument stability issue for current and future lots, reduced On-board Instrument Stability from 7 days to 5 days
The recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed.
Specific Pumps may exhibit intermittent performance in the AILD (Air in Line Detector) function. If an AILD does not sufficiently discern fluid from air in line, an air in line event may…
The rear heater plate and cover assembly that contains the electrical wiring for the heaters does not have sufficient bonding to ground.
There was an increase in complaints related to tip breaks and wobble/vibration.
Under certain conditions, some slices may be missing which can lead to a gap of anatomy in the 3D Volume images.
Labeled On-board instrument stability issue for current and future lots, reduced On-board Instrument Stability from 7 days to 5 days
VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Quantitative Controls Outside of Expected Control Range, potential for delayed results
Firm unable to confirm that the tenaculum devices were produced in accordance with required design and manufacturing standards.
Firm unable to confirm that the tenaculum devices were produced in accordance with required design and manufacturing standards.
There is a potential that the length of bone screws identified on labeling may not correspond to the actual length of the screw included.
There was an increase in complaints related to tip breaks and wobble/vibration.
Labeled On-board instrument stability issue for current and future lots, reduced On-board Instrument Stability from 7 days to 5 days
There was an increase in complaints related to tip breaks and wobble/vibration.
Ancillary reagent packs used on Atellica IM 1300 and Atellica IM 1600 analyzers may overflow when pierced while on an analyzer located at an altitude of greater than 350m (1148ft) above sea…
Firm unable to confirm that the tenaculum devices were produced in accordance with required design and manufacturing standards.
Under certain conditions, some slices may be missing which can lead to a gap of anatomy in the 3D Volume images.
Under certain conditions, some slices may be missing which can lead to a gap of anatomy in the 3D Volume images.
Under certain conditions, some slices may be missing which can lead to a gap of anatomy in the 3D Volume images.
Product has a lack of sterility assurance
Due to unapproved raw materials used in the manufacturing of Covid-19 control pack, their is the potential for delayed amplification signals.
Ultrasound system software issue can cause an EchoNavigator error notification, leading to an unresponsive system, necessitating system restart, which could lead to therapy/treatment delay…
Under certain conditions, some slices may be missing which can lead to a gap of anatomy in the 3D Volume images.
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.
