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. 3,031 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,031 in last 12 months

Showing 69416960 of 30,923 recalls

Medical DeviceApril 10, 2023· Wright Medical Technology, Inc.

Recalled Item: stryker ORTHOLOC 3Di Fusion Plate MTP Right Recalled by Wright Medical...

The Issue: Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2023· Cytrellis Biosystems, Inc.

Recalled Item: Cytrellis ellacor System with Micro-Coring Technology-Dermal Micro-Coring...

The Issue: Irregular core patterns could cause potential overlap of cores at the 8%...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2023· Cook Incorporated

Recalled Item: Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Tray Recalled by...

The Issue: There were reports from customers that the tracheostomy in the sets and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 7, 2023· Cook Incorporated

Recalled Item: Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set Recalled by...

The Issue: There were reports from customers that the tracheostomy in the sets and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 6, 2023· Karl Storz Endoscopy

Recalled Item: Metal Tray Recalled by Karl Storz Endoscopy Due to Metal sterilization trays...

The Issue: Metal sterilization trays used to encase and protect medical devices during...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2023· Elekta, Inc.

Recalled Item: Elekta Unity Image-Guided Radiation Therapy System containing an MR gradient...

The Issue: There is a low possibility that an electrical connector in the MR gradient...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2023· 3M Company - Health Care Business

Recalled Item: 3M Attest Steam Chemical Integrators Recalled by 3M Company - Health Care...

The Issue: 3M Attest Steam Chemical Integrators with dates of manufacture between...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2023· Fisher Wallace Laboratories Inc.

Recalled Item: Fisher Wallace Stimulator Models FW-100 and FW-200 Recalled by Fisher...

The Issue: If the batteries are installed incorrectly, the product may overheat,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2023· Hiossen Inc.

Recalled Item: ET III Nano-HA fixture System ET NH Dental Implant Model Recalled by Hiossen...

The Issue: Mis-labeled length of the dental implant on the Recall Implant's package....

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2023· 3M Company - Health Care Business

Recalled Item: 3M Attest Steam Chemical Integrators Recalled by 3M Company - Health Care...

The Issue: 3M Attest Steam Chemical Integrators with dates of manufacture between...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation ES (Med ES Main) Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to an automated dispensing cabinet software issue, when a medication...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Illumina, Inc.

Recalled Item: MiSeq Dx Instrument Recalled by Illumina, Inc. Due to Cybersecurity...

The Issue: Cybersecurity vulnerability concerning the software used for sequencing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Karl Storz Endoscopy

Recalled Item: KARL STORZ Radel Sterilization Trays Recalled by Karl Storz Endoscopy Due to...

The Issue: Plastic sterilization trays used to encase and protect medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Illumina, Inc.

Recalled Item: NextSeq 550Dx Instrument Recalled by Illumina, Inc. Due to Cybersecurity...

The Issue: Cybersecurity vulnerability concerning the software used for sequencing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Toxicology Calibrator (TOX CAL)-The Atellica¿ CH Toxicology...

The Issue: Reassignment of the Atellica CH Toxicology Calibrators (TOX CAL) and ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry ToxAmmonia Calibrator- In vitro diagnostic use in the...

The Issue: Reassignment of the Atellica CH Toxicology Calibrators (TOX CAL) and ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Smiths Medical ASD Inc.

Recalled Item: DuraLife Autoclavable Double Swivel Elbow Recalled by Smiths Medical ASD...

The Issue: DuraLife devices instructions for cleaning and sterilization have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Bicarbonate Recalled by Beckman Coulter Inc. Due to There is...

The Issue: There is a potential for a decrease in calibration ODs for Bicarbonate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Bicarbonate Recalled by Beckman Coulter Inc. Due to There is...

The Issue: There is a potential for a decrease in calibration ODs for Bicarbonate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Smiths Medical ASD Inc.

Recalled Item: DuraLife Autoclavable Silicone Extension Tube Recalled by Smiths Medical ASD...

The Issue: DuraLife devices instructions for cleaning and sterilization have been...

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

Class II — Potential Health HazardOngoing