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.
62,271published records in database
4recall categories represented
Sep 4, 2019newest stored source record
Latest records
Latest recalls — page 1170
The newest recall records with useful source details are listed here.
Performance issues with certain lots of the Elecsys Anti-CCP assay on the cobas e 411 analyzer; MODULAR ANALYTICS E 170 module; and cobas e 601, 602, and 801 modules with plasma samples.
Class IIFDA: TerminatedRoche Diagnostics Operations, Inc.
Monaco is displaying the Anatomy and Beam shift direction incorrectly on the Monaco Scan and Setup Reference Report and is DICOM exporting incorrect (Anatomy/Beam) shift directions.
The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.
Class IIFDA: TerminatedBard Peripheral Vascular Inc.
The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.
Class IIFDA: TerminatedBard Peripheral Vascular Inc.
Supplemental information provided with devices may indicate that the subdural electrodes, depth electrodes, and anchor bolts are approved for use in the MR environment, for which they are…
Class IIFDA: TerminatedAd-Tech Medical Instrument Corporation
The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.
Class IIFDA: TerminatedBard Peripheral Vascular Inc.
The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.
Class IIFDA: TerminatedBard Peripheral Vascular Inc.
The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.
Class IIFDA: TerminatedBard Peripheral Vascular Inc.
The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.
Class IIFDA: TerminatedBard Peripheral Vascular Inc.
Salivary Progesterone assay may observe a higher percentage of samples with low results. Saliva samples in the low measuring range of the kit {< 20 pg/ml) were assayed and producing a…
The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.
Class IIFDA: TerminatedBard Peripheral Vascular Inc.
The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.
Class IIFDA: TerminatedBard Peripheral Vascular Inc.
The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.
Class IIFDA: TerminatedBard Peripheral Vascular Inc.
The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.
Class IIFDA: TerminatedBard Peripheral Vascular Inc.
The firm updated the IFU in April 2019 to clarify that use of the TRANSWARMER Mattress with other heat producing devices, such as an incubator, is prohibited and could lead to serious…
Class IIFDA: TerminatedCooperSurgical, Inc.
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