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 2338123400 of 30,923 recalls

Medical DeviceSeptember 28, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Calibrator Kit 9 Calibrator Recalled by...

The Issue: The firm is conducting a product correction due to an increase in U90-382 or...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2015· Varian Medical Systems, Inc.

Recalled Item: ARIA Radiation Oncology Recalled by Varian Medical Systems, Inc. Due to An...

The Issue: An anomaly was identified with the ARIA for Radiation Oncology software with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2015· GE Healthcare

Recalled Item: The Centricity Universal Viewer Version is a device that displays Recalled...

The Issue: Inaccurate distance measurements with magnified projection X-ray images.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2015· Synthes (USA) Products LLC

Recalled Item: Synthes 2.7MM/3.5MM VA-LCP Medial Distal Humerus Plates 10H/RT/186mm-...

The Issue: The 2.7MM/3.5MM VA-LCP Humerus Plates were found to be labeled incorrectly....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2015· GE Healthcare

Recalled Item: The Centricity PACS-IW with Universal Viewer is a device that Recalled by GE...

The Issue: Inaccurate distance measurements with magnified projection X-ray images.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2015· Stryker Spine

Recalled Item: Stryker Radius 5.5 to 3.5 Rod to Red Connector Recalled by Stryker Spine Due...

The Issue: Stryker Spine is recalling Radius Rod to Rod Connector 5.5 to 3.5 mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Hemoglobin A1c_3 Recalled by Siemens Healthcare Diagnostics,...

The Issue: Reagent in these lots may demonstrate an increased occurrence of high %HbA1c...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2015· Airways Development LLC

Recalled Item: Airways Development LLC WaterPAP Positive Airway Pressure Device #WP-7700....

The Issue: Airways Development LLC has received a complaint about a canister leaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2015· GE Medical Systems, LLC

Recalled Item: MR Surgical Suite II Table Recalled by GE Medical Systems, LLC Due to GE...

The Issue: GE became aware of an issue with the table transfer release mechanism of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2015· Instrumentation Industries Inc

Recalled Item: Ventilator Tubing Recalled by Instrumentation Industries Inc Due to As a...

The Issue: As a distributor of tubing manufactured by Smooth Bore Plastics, we are...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2015· Ethicon Endo-Surgery Inc

Recalled Item: HARMONIC ACE+ 7 Laparoscopic Shears with Advanced Hemostasis (23cm Recalled...

The Issue: Complaints of holes in Tyvek which can compromise the sterile barrier...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2015· Berchtold Corp.

Recalled Item: TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is Recalled by...

The Issue: During the use of the TELETOM Series 4 & 6 there is potential for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2015· ELITech Clinical Systems SAS

Recalled Item: Envoy 500 system includes the following product numbers and Recalled by...

The Issue: ELITech clinical Systems reagents based on Trinder reaction used on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2015· ELITech Clinical Systems SAS

Recalled Item: Eon 100 system included the following product numbers and Recalled by...

The Issue: ELITech clinical Systems reagents based on Trinder reaction used on the Eon...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2015· ELITech Clinical Systems SAS

Recalled Item: Eon 300 system includes the following product numbers and Recalled by...

The Issue: ELITech clinical Systems reagents based on Trinder reaction used on the Eon...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2015· ELITech Clinical Systems SAS

Recalled Item: ELITech Clinical Systems reagents used on the Selectra ProS and Recalled by...

The Issue: ELITech Clinical Systems reagents based on Trinder reaction used on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2015· Sentinel CH SpA

Recalled Item: Sentinel MULTIGENT Ammonia Ultra Reagent Recalled by Sentinel CH SpA Due to...

The Issue: Results for ammonia are below the linear range of the assay for samples that...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2015· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. Product Usage: Merge Cardio is a system Recalled by...

The Issue: Users can merge a device import file with an image study that already has a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2015· Biocompatibles U.K., Ltd.

Recalled Item: TheraSphere(R) YTTRIUM-90 CLASS MICROSPHERE INJECTION TheraSphere¿ is...

The Issue: One mislabeled dose of TheraSphere¿ Y-90 Glass Microspheres, which was...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2015· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Duracon Flat Tibial Wedge Cemented use only Sterile....

The Issue: Stryker Orthopaedics has received two customer complaints regarding Duracon...

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

Class II — Potential Health HazardOngoing