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.
When connected to the Mission Critical (MC) and /or Information Exchange (IX) networks, certain versions of the CARESCAPE Telemetry Server, ApexPro Telemetry Server, CARESCAPE Central…
A positive bias was confirmed to exists on the STA - Unicalibrator levels with STA - Deficient IX and STA - Deficient VIII when compared to the International Standard (IS) for factor VIII…
There is a potential performance issue as detected by an under-recovery of sample results during routine testing.
Editing a static arc beam may unexpectedly set the MU of the beam to its initial default value of 200 MU. If the bug is triggered, the dose is invalidated and needs to be recalculated…
The firm has become aware that the Snapshot Trackers were not manufactured in accordance with specifications and could potentially lead to navigational inaccuracies, which may result in…
When connected to the Mission Critical (MC) and /or Information Exchange (IX) networks, certain versions of the CARESCAPE Telemetry Server, ApexPro Telemetry Server, CARESCAPE Central…
There is a potential performance issue as detected by an under-recovery of sample results during routine testing.
When connected to the Mission Critical (MC) and /or Information Exchange (IX) networks, certain versions of the CARESCAPE Telemetry Server, ApexPro Telemetry Server, CARESCAPE Central…
Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents due to incorrect MRI information on the IFU. The correct classification is "MRI Conditional" not "MRI Safe".
Sentiva generators may reset and become disabled within 60 days of enabling. Physicians can re-enable but devices will continue to be susceptible to resets. If a device experiences this…
This lot of test strips is showing an under-recovery when tested against a reference method.
Potential for one of the four temporal electrode cables used in with the ElectroTek EEG system having incorrect placement labels which could lead to incorrect placement of electrode for an…
During the firm's review of May 2019 complaint data, a significant increase in Disposable Core Biopsy Instrument complaints were observed for Failure to Fire, Firing Problem, and Failure to…
RTE products potentially contaminated with Listeria monocytogenes.
Incorrect product label on back panel, undeclared cashew, pecan, milk and soy
RTE products potentially contaminated with Listeria monocytogenes.
Products recalled due to possible contamination with Listeria monocytogenes
RTE products potentially contaminated with Listeria monocytogenes.
RTE products potentially contaminated with Listeria monocytogenes.
Products have the potential to cause scombrotoxin fish poisoning because they may have increased levels of histamine.
Products have the potential to cause scombrotoxin fish poisoning because they may have increased levels of histamine.
RTE products potentially contaminated with Listeria monocytogenes.
RTE products potentially contaminated with Listeria monocytogenes.
RTE products potentially contaminated with Listeria monocytogenes.
Browse recent months with enough recall history for useful comparison.
