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 2422124240 of 56,506 recalls

DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sulfur Colloid Reaction Vial 1.0 mL Recalled by Synthetopes Inc Due to Lack...

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sn-DTPA Kit 10 mg Recalled by Synthetopes Inc Due to Lack of Processing...

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sn-DMSA solution Recalled by Synthetopes Inc Due to Lack of Processing Controls.

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sn-Tetrofosmin Kit 5.0 mL Recalled by Synthetopes Inc Due to Lack of...

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sn-Pyrophosphate Kit Recalled by Synthetopes Inc Due to Lack of Processing...

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sn-d Recalled by Synthetopes Inc Due to Lack of Processing Controls.

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sn-Mertiatide Kit Recalled by Synthetopes Inc Due to Lack of Processing...

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 28, 2019· Nobel Biocare Usa Llc

Recalled Item: Healing Abutment Conical Connection RP 0 3.6 x 5mm Recalled by Nobel Biocare...

The Issue: Packaged dental implant healing abutments were found to contain the wrong...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Medline Industries Inc

Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 10 Fr 3 ml Recalled by...

The Issue: Loose silicone particulate was found to be present on the shaft of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Medline Industries Inc

Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 8 Fr 3 ml Recalled by...

The Issue: Loose silicone particulate was found to be present on the shaft of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Medline Industries Inc

Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 6 Fr 1.5 ml Recalled by...

The Issue: Loose silicone particulate was found to be present on the shaft of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Sheridan/HVT: 1) Novaplus 7.0 mm Recalled by Teleflex Medical Due to This...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan: 1) Uncuffed 6.0 mm Recalled by Teleflex Medical Due to...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Cook Inc.

Recalled Item: Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm Recalled by...

The Issue: Multiple complaints were received for balloons bursting below the rated...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan: 1) Preformed 6.0 mm Recalled by Teleflex Medical Due to...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Cook Inc.

Recalled Item: Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm Recalled by...

The Issue: Multiple complaints were received for balloons bursting below the rated...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Cook Inc.

Recalled Item: Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm Recalled by...

The Issue: Multiple complaints were received for balloons bursting below the rated...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan LTS Recalled by Teleflex Medical Due to This voluntary...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Sheridan/CF Novaplus 7.0 mm Recalled by Teleflex Medical Due to This...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan: 1) HVT 6.0 mm Recalled by Teleflex Medical Due to This...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing