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. 2,811 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,811 in last 12 months

Showing 3550135520 of 56,506 recalls

Medical DeviceOctober 5, 2016· Oscor, Inc.

Recalled Item: OSCOR ADELANTE BREEZWAY 10F STRAIGHT S79CM D84CM Catalog # AB101219 Recalled...

The Issue: Complaint that during insertion of the dilator through the sheath a fragment...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· Oscor, Inc.

Recalled Item: OSCOR BREEZEWAY 10F S60.8CM D65.6CM FIRM TIP Catalog # AB1061FT Recalled by...

The Issue: Complaint that during insertion of the dilator through the sheath a fragment...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· Oscor, Inc.

Recalled Item: MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C90¿ S61CM D66CM GLOBAL...

The Issue: Complaint that during insertion of the dilator through the sheath a fragment...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· Oscor, Inc.

Recalled Item: OSCOR ADELANTE BREEZEWAY 10F C120¿ S61CM D66CM Catalog # AB101075 Recalled...

The Issue: Complaint that during insertion of the dilator through the sheath a fragment...

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

Class II — Potential Health HazardOngoing
FoodOctober 5, 2016· King Henry's, Inc.

Recalled Item: Gummy Frogs Recalled by King Henry's, Inc. Due to Undeclared Colors

The Issue: King Henry is recalling King Henry's Gummy Frogs because they may contain...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 5, 2016· Professional Botanicals

Recalled Item: Professional Botanicals MealPlex (756 grams) and Veo Natural Pearl 3.0...

The Issue: Professional Botanicals announces a voluntary field action for MealPlex and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 5, 2016· King Henry's, Inc.

Recalled Item: Gummy Frogs Recalled by King Henry's, Inc. Due to Undeclared Colors

The Issue: King Henry is recalling King Henry's Gummy Frogs because they may contain...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 4, 2016· Del Monte Research Center - Walnut Creek

Recalled Item: DM Light Slices Yellow Cling Peaches -15 oz (425g) 300 x 407 Recalled by Del...

The Issue: Between September 7 thru September 29, 2016, consumer complaints led firm to...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 4, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: COBAS INTEGRA 800 Tina-Quant Hemoglobin A1cDX Gen.2 Hemoglobin A1cDX test...

The Issue: .Roche Diagnostics has confirmed elevated QC and patient sample recovery for...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2016· Medtronic

Recalled Item: Covidien Clearify Visualization System Item Code: 21-345 Intended to be...

The Issue: Product sterility is compromised due to breach of the sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2016· Medtronic

Recalled Item: Best Practices kits containing certain production lots of Clearify...

The Issue: Product sterility is compromised due to breach of the sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Tina-Quant Hemoglobin A1c Gen. 2 Hemoglobin A1c test Catalog number Recalled...

The Issue: Roche Diagnostics has confirmed elevated QC and patient sample recovery for...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2016· Nurse Assist, Inc

Recalled Item: Normal Saline Flush 0.9% USP Sodium Chloride Injection Syringe Recalled by...

The Issue: Potential contamination with B. cepacia.

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 3, 2016· Synthes (USA) Products LLC

Recalled Item: 3.0 mm Reaming Rod/950 mm Recalled by Synthes (USA) Products LLC Due to The...

The Issue: The peel pouches for the affected reaming rods and extraction hooks are...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2016· Medimaps Group

Recalled Item: TBS iNsight Version v.3.0.1 Product Usage: TBS iNsight is a Recalled by...

The Issue: The FRAX adjusted for TBS values are not correct when: The FRAX feature is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2016· Medtronic Neuromodulation

Recalled Item: Model 37751 Recharger Product Usage: The Medtronic 37751 Recharger is...

The Issue: Medtronic has identified an increased number of complaints from customers...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2016· Synthes (USA) Products LLC

Recalled Item: 2.5 mm Reaming Rod W/Ball Tip 650 mm Recalled by Synthes (USA) Products LLC...

The Issue: The peel pouches for the affected reaming rods and extraction hooks are...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2016· Synthes (USA) Products LLC

Recalled Item: Extraction Hook - Sterile for TI Cannulated Nails Recalled by Synthes (USA)...

The Issue: The peel pouches for the affected reaming rods and extraction hooks are...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2016· Synthes (USA) Products LLC

Recalled Item: 2.5 mm TI Calibrated Reaming Rod 850 mm Recalled by Synthes (USA) Products...

The Issue: The peel pouches for the affected reaming rods and extraction hooks are...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2016· Synthes (USA) Products LLC

Recalled Item: 2.5 mm Reaming Rod with Ball Tip & Extension/950 mm Recalled by Synthes...

The Issue: The peel pouches for the affected reaming rods and extraction hooks are...

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

Class II — Potential Health HazardOngoing