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.
20 Pumps sold to the Finnish market contain a message in which one word in the message is mistranslated. When the user follows a specific set of key presses the pump will display the…
Terumo CVS initiated a voluntary recall for the Level Sensor II Pads and Level Sensor Gel Pads due to non-compliant labeling because the product expiration date is displayed in a format…
CareFusion is recalling the MaxGuard Extension Set with Injection Site and 0.2 micron filter because of reports of separation and/or leakages between the Y-connector and tubing.
Reports that the sample type "cord blood" has been changed into the two sample types "cord blood arterial" and "cord blood venous.
Four issues: 1. Motion controller problem stops scan and no data image produced. 2. Door interlock switch problem disables CT scan. 3. Detector contacts head holder when performing Patient…
A gap in the housing of the wireless foot switch could potentially result in liquids penetrating the interior. Such liquids may include disinfectants, cleaning agents and/ or bodily fluids.…
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
The Controller Cap of the C2 CyroBalloon Ablation System may crack as it is tightened onto the controller. That could compromise the integrity and result in damage to the Controller Cap.
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
A gap in the housing of the wireless foot switch could potentially result in liquids penetrating the interior. Such liquids may include disinfectants, cleaning agents and/ or bodily fluids.…
Spacelabs has received reports of the Arkon Anesthesia Delivery System, Model 99999, shutting down without warning. The power supply has failed in a way that does not trigger the normal on…
Intermittent imprecision in results generated using two specific lots of VITROS Li Slides.
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
Terumo CVS initiated a voluntary recall for the Level Sensor II Pads and Level Sensor Gel Pads due to non-compliant labeling because the product expiration date is displayed in a format…
It was discovered that the generator of the system could possibly terminate the exposure prematurely during an examination
Maquet has received several complaints involving the VASOVIEW HEMOPRO VH-3500 which involve the device exhibiting the failure mode of intermittent or no power.
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
Reports that the sample type "cord blood" has been changed into the two sample types "cord blood arterial" and "cord blood venous.
Smiths Medical became aware that one lot of the Bivona 3.5mm TTS Cuffed Pediatric tracheostomy tubes was incorrectly labeled for neonatal use instead of correctly labeled for pediatric…
Browse recent months with enough recall history for useful comparison.
