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. 3,026 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,026 in last 12 months

Showing 89018920 of 30,923 recalls

Medical DeviceFebruary 2, 2022· Philips Healthcare

Recalled Item: Philips StentBoost Live R2.0 application Recalled by Philips Healthcare Due...

The Issue: Due to an incorrect configuration setting in the EPX database of StentBoost...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2022· Philips North America Llc

Recalled Item: Philips Allura (Model Numbers 722010 Recalled by Philips North America Llc...

The Issue: Due to a software defect, the Philips StentBoost Live R2.0 might not process...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2022· Ace Surgical Supply Co., Inc.

Recalled Item: NuOss Collagen Block Size 8mm x 9mm x 9mm- used Recalled by Ace Surgical...

The Issue: NuOss Collagen (dental) was packaged with a Collatene Fibrillar Collagen(for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BSN Medical Inc

Recalled Item: (1) JOBST Compri2 Recalled by BSN Medical Inc Due to Mislabeling

The Issue: The folding boxes within the shipping case are mislabeled. The shipping case...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· Mevion Medical Systems, Inc.

Recalled Item: Mevion S250 and S250i Proton Therapy Systems hand pendant (P/N Recalled by...

The Issue: Malfunction of the hand pendant controlling movement of the therapy couch...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC M/L Recalled by BioPro,...

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MD Recalled by BioPro,...

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant)TOE JOINT TITANIUM NPC LG Recalled by BioPro, Inc....

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MS Recalled by BioPro, Inc....

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC SM Recalled by BioPro,...

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC LG Recalled by BioPro, Inc....

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant)TOE JOINT TITANIUM PC SM Recalled by BioPro, Inc....

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC ML Recalled by BioPro,...

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MS Recalled by BioPro,...

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2022· BioPro, Inc.

Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MD Recalled by BioPro, Inc....

The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2022· Canon Medical System, USA, INC.

Recalled Item: INFX-8000V. For radiographic and fluoroscopic studies and intervention....

The Issue: The fluoroscopic dose rate might exceed the conforming value during biplane...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Ysiosystem with VC10 software version Recalled by Siemens Medical Solutions...

The Issue: Siemens Healthineers has identified a software error in previous software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2022· SD Biosensor, Inc.

Recalled Item: STANDARD Q COVID-19 Ag Home Test STANDARD Q COVID-19 Ag Recalled by SD...

The Issue: Illegal importation of COVID-19 AG Test kits into the U.S. The COVID-19 Ag...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 31, 2022· B. Braun Medical, Inc.

Recalled Item: Dispensing Pins for Air Inlet Filter Recalled by B. Braun Medical, Inc. Due...

The Issue: This lot may have an elevated risk of leakage from the Air-Inlet Filter of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2022· B Braun Medical Inc

Recalled Item: Conductivity Sensors utilized on Dialog and Dialog+ Hemodialysis Systems....

The Issue: Firm learned of the potential for cracks to form in the conductivity sensors...

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

Class II — Potential Health HazardOngoing