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. 2,851 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,851 in last 12 months

Showing 2474124760 of 30,923 recalls

Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange PhysioMesh Flexible Composite Mesh 15 x 15cm...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry XPT System Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: Siemens Healthcare Diagnostics has confirmed an issue with ADVIA Chemistry...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange 12x40 Airway Stent System Recalled by EXP...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange - Trocar VersaPort Plus V2 Recalled by EXP...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange 3.5mm Threaded Cerclage Pin Recalled by EXP...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange Angio-Seal VIP Platform/Vascular Closure Device 6F...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange - Auto Suture Endo Universal 65¿¿ 4mm Recalled by...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange PT WIRE 300 Recalled by EXP Pharmaceutical Services...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· Intuitive Surgical, Inc.

Recalled Item: EndoWrist One Vessel Sealer Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Intuitive Surgical has identified the potential for a certain, small portion...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange TAUT Intraducer Peritoneal Catheter 2mm x 1.6mm x...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· Sybron Dental Specialties

Recalled Item: Outer cardboard box labeling: Pinnacle Cure Sleeve Recalled by Sybron Dental...

The Issue: Cases of Cure Sleeve labeled with part number 4513, which fits 13mm tips,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· DePuy Orthopaedics, Inc.

Recalled Item: SMARTSET GHV Gentamicin Bone Cement. A self-curing Recalled by DePuy...

The Issue: One lot of SMARTSET GHV Gentamicin Bone Cement is partially agglomerated ....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· Intuitive Surgical, Inc.

Recalled Item: EndoWrist One Vessel Sealer Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Intuitive Surgical has identified the potential for a certain, small portion...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange 10x40 Airway Stent System Recalled by EXP...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange - 5.5mm BioComposite Corkscrew FT Recalled by EXP...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange 12MM VASCULAR Recalled by EXP Pharmaceutical...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2015· Tosoh Bioscience, Inc.

Recalled Item: G7 Variant Elution Buffer HiS no. 1 (M) component of Recalled by Tosoh...

The Issue: The G7 Variant Elution Buffer HiS no. 1 (M) is incorrectly labeled with an...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 9, 2015· CooperSurgical, Inc.

Recalled Item: CooperSurgical PESSARY KIT-CUBE#2 Recalled by CooperSurgical, Inc. Due to...

The Issue: Incorrect size printed on the Milex Pessary Kit packaging label

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare DigitalDiagnost System X-Ray Recalled by Philips Medical...

The Issue: The system is designed to emit a beep upon termination of an exposure....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare DuraDiagnost X- Ray Recalled by Philips Medical Systems,...

The Issue: The system is designed to emit a beep upon termination of an exposure....

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

Class II — Potential Health HazardOngoing