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. 2,828 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,828 in last 12 months

Showing 3224132260 of 56,506 recalls

Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: Lateral Troch Plate Full Crimp - 254mm Recalled by Zimmer Biomet, Inc. Due...

The Issue: Possibility that the patient label inside the product box was incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: RED SEXP DSTL FEM 19CM RT ASSY Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Possibility that the patient label inside the product box was incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: CER OPTION TYPE 1 TPR SLEVE -6 Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Possibility that the patient label inside the product box was incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: COMP 12MM HUM FRAC STEM MACRO Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Possibility that the patient label inside the product box was incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: OSS CEMENTED IM STEM 12X150 Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Possibility that the patient label inside the product box was incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: RED SEXP DSTL FEM 19CM LT ASSY Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Possibility that the patient label inside the product box was incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: COMP PRIMARY STEM 8MM MINI Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Possibility that the patient label inside the product box was incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: CER BIOLOXD OPTION HD 32MM Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Possibility that the patient label inside the product box was incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: Lateral Troch Plate Full Crimp - 254mm Recalled by Zimmer Biomet, Inc. Due...

The Issue: Possibility that the patient label inside the product box was incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: ECHO POR FMRL NC 9X125 Recalled by Zimmer Biomet, Inc. Due to Possibility...

The Issue: Possibility that the patient label inside the product box was incorrectly...

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

Class II — Potential Health HazardOngoing
DrugJune 2, 2017· G & W Laboratories, Inc.

Recalled Item: G & W Clobetasol Propionate Ointment 0.05% Recalled by G & W Laboratories,...

The Issue: Failed impurities/degradation specifications: This product is being recalled...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 2, 2017· Sterilmed Inc

Recalled Item: St. Jude Medical. Agilis NxT Steerable Introducer: B1-Directional Recalled...

The Issue: Inadequate seal due to lack of adhesive glue

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 2, 2017· C.R. Bard, Inc.

Recalled Item: BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension Recalled...

The Issue: Customer complaint of a cut in the side of the leg bag, indicating a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Infinity 7 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Infinity 5 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Infinity 7 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Proclaim 7 Elite Recalled by St. Jude Medical, Inc. Due to The firm...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Infinity 5 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Proclaim 5 Elite Recalled by St. Jude Medical, Inc. Due to The firm...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
DrugJune 1, 2017· American Pharmaceutical Ingredients LLC

Recalled Item: Doxycycline Hyclate USP Recalled by American Pharmaceutical Ingredients LLC...

The Issue: Labeling: Not Elsewhere Classified. Manufacturer and product were discovered...

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

Class II — Potential Health HazardOngoing
Refund