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. 3,072 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,072 in last 12 months

Showing 401420 of 56,506 recalls

Medical DeviceDecember 23, 2025· Focalyx Technologies, LLC.

Recalled Item: Focalyx Fusion Recalled by Focalyx Technologies, LLC. Due to Software device...

The Issue: Software device that is an accessory for image-guided interventional and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2025· Medline Industries, LP

Recalled Item: Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE...

The Issue: These lots of reprocessed catheters may contain small particles of residual...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2025· Medline Industries, LP

Recalled Item: Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheters:...

The Issue: These lots of reprocessed catheters may contain small particles of residual...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2025· Medline Industries, LP

Recalled Item: Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheters:...

The Issue: These lots of reprocessed catheters may contain small particles of residual...

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

Class I — Serious Health HazardOngoing
DrugDecember 22, 2025· Cipla USA, Inc.

Recalled Item: Diclofenac Sodium Topical Gel Recalled by Cipla USA, Inc. Due to Failed PH...

The Issue: Failed PH Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugDecember 22, 2025· Baxter Healthcare Corporation

Recalled Item: Sterile Water for Irrigation Recalled by Baxter Healthcare Corporation Due...

The Issue: Presence of particulate matter: plastic particles from the bottle rim were...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 22, 2025· Medline Industries, LP

Recalled Item: Reprocessed St. Jude Supreme and Response Diagnostic Electrophysiology...

The Issue: These lots of reprocessed catheters may contain small particles of residual...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2025· Medline Industries, LP

Recalled Item: Reprocessed Siemens ACUSON AcuNav Diagnostic Ultrasound Catheters: ACUSON...

The Issue: These lots of reprocessed catheters may contain small particles of residual...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2025· Medline Industries, LP

Recalled Item: Reprocessed Abbott Inquiry Steerable Diagnostic Catheters: Abbott Inquiry...

The Issue: These lots of reprocessed catheters may contain small particles of residual...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2025· Medline Industries, LP

Recalled Item: Medline ReNewal Reprocessed Webster CS Catheters: Webster CS Catheter 10...

The Issue: These lots of reprocessed catheters may contain small particles of residual...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2025· LSL Healthcare Inc.

Recalled Item: LSL Healthcare Recalled by LSL Healthcare Inc. Due to BD ChloraPrep Triple...

The Issue: BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2025· Philips North America

Recalled Item: Patient Information Center iX Recalled by Philips North America Due to A...

The Issue: A recent software (SW) patch modifies Mobile Event Notification filter...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM X.ceed Software applications: syngo.CT Brain Quantification syngo.CT...

The Issue: To remove the software applications from certain CT systems as the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery-Enhanced Delivery System - 6mm x 8mm Recalled...

The Issue: Increased reports of stent deployment and expansion issues. The most common...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2025· Boston Scientific Corporation

Recalled Item: *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 8mm x 8mm...

The Issue: Increased reports of stent deployment and expansion issues. The most common...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: NAEOTOM Alpha.Pro Software applications: syngo.CT Brain Quantification...

The Issue: To remove the software applications from certain CT systems as the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Boston Scientific Corporation

Recalled Item: HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 6mm x 8mm...

The Issue: Increased reports of stent deployment and expansion issues. The most common...

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

Class I — Serious Health HazardOngoing
DrugDecember 19, 2025· Sato Pharmaceutical Co., Ltd

Recalled Item: INON ACE Antacid tablets (magnesium aluminosilicate Recalled by Sato...

The Issue: Failed Disintegration Specifications: above the time expected.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 19, 2025· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery-Enhanced Delivery System - 20mm x 10mm...

The Issue: Increased reports of stent deployment and expansion issues. The most common...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2025· Altruan GmbH

Recalled Item: Wondfo Streptococcal A At-Home Self-Test. At-home test for group A Recalled...

The Issue: Product not cleared by the FDA.

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

Class II — Potential Health HazardOngoing