Product Recalls in California

Product recalls affecting California — including food, drugs, consumer products, medical devices, and vehicles distributed to California. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,881 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,881 in last 12 months

Showing 2114121160 of 30,923 recalls

Medical DeviceAugust 15, 2016· Pentax of America Inc

Recalled Item: Pentax Video Gastroscope is intended to be used with a Recalled by Pentax of...

The Issue: PENTAX Medical is initiating this field action to provide customers that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2016· Microgenics Corporation

Recalled Item: Thermo Scientific QMS Everolimus Assay Recalled by Microgenics Corporation...

The Issue: A reagent stability issue (still under investigation) causes less separation...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2016· Novarad Corporation

Recalled Item: NovaPACS versions 8.4.7 Recalled by Novarad Corporation Due to Novarad...

The Issue: Novarad Corporation announces a voluntary field action for the NovaPACS...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2016· Medtronic Inc., Cardiac Rhythm and Heart Failure

Recalled Item: Medtronic Recalled by Medtronic Inc., Cardiac Rhythm and Heart Failure Due...

The Issue: 78 Viva CRT -Ds and Evera ICDs that were manufactured with a specific subset...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2016· Arthrex, Inc.

Recalled Item: Arthrex Suture Washer Recalled by Arthrex, Inc. Due to The device was...

The Issue: The device was assembled incorrectly. Suture and washer were not assembled;...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceAugust 12, 2016· Merit Medical Systems, Inc.

Recalled Item: Custom Fluid Management Set Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Merit Medical Systems, Inc. announces a voluntary field action for Fluid...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2016· Philips Electronics North America Corporation

Recalled Item: PCR Compano Basic Reader using 100-127V as mains voltage. Model numbers:...

The Issue: A defect component of the Compano reader power supply can cause the power...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2016· Medtronic Inc., Cardiac Rhythm and Heart Failure

Recalled Item: Medtronic Recalled by Medtronic Inc., Cardiac Rhythm and Heart Failure Due...

The Issue: 78 Viva CRT -Ds and Evera ICDs that were manufactured with a specific subset...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2016· Maquet Cardiovascular Us Sales, Llc

Recalled Item: The Connecting Bracket (Fixture) Device (1002.65A0) is designed as a...

The Issue: Post Market Surveillance cases reported to Maquet showing instances in which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2016· Ortho Kinematics, Inc

Recalled Item: Vertebral Motion Analyzer (VMA) Recalled by Ortho Kinematics, Inc Due to...

The Issue: Ortho Kinematics, Inc. notified customers of erroneous results of VMA tests...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDLab 1265 Blood Gas Analyzer Siemens Material Number (SMN): 10321852...

The Issue: There is a potential for the first and/or last name of one patient to be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Synergetics Inc

Recalled Item: 25 gauge VersaVit 2.0 Core Essentials Procedure Pack Recalled by Synergetics...

The Issue: Vitrectomy cutters have been found not to be operating within the correct...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDLab 1260 Blood Gas Analyzer Siemens Material Number (SMN): 10321846...

The Issue: There is a potential for the first and/or last name of one patient to be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDLab 1240 Blood Gas Analyzer Siemens Material Number (SMN):...

The Issue: There is a potential for the first and/or last name of one patient to be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products GLU Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Ortho Clinical Diagnostics confirmed that N-Acetylcysteine (NAC), a drug...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products LAC Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Ortho Clinical Diagnostics confirmed that N-Acetylcysteine (NAC), a drug...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint¿ 400 Blood Gas Analyzer Siemens Material Number (SMN):...

The Issue: There is a potential for the first and/or last name of one patient to be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Blood Gas Analyzer Siemens Material Number (SMN):...

The Issue: There is a potential for the first and/or last name of one patient to be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Synergetics Inc

Recalled Item: 25 gauge VersaVit 2.0 Vitrectomy Cutter Recalled by Synergetics Inc Due to...

The Issue: Vitrectomy cutters have been found not to be operating within the correct...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDLab 1245 Blood Gas Analyzer Siemens Material Number (SMN): 10321844...

The Issue: There is a potential for the first and/or last name of one patient to be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing