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. 3,022 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,022 in last 12 months

Showing 95219540 of 56,506 recalls

FoodJune 12, 2023· S. Martinelli Harvest Facility

Recalled Item: Martinelli's Gold Medal 100% Apple Juice 10 oz. glass bottles Recalled by S....

The Issue: Potential glass quality issue that may result in glass chips in the product

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 12, 2023· Gelato Boy

Recalled Item: Gelato Boy Chocolate Chunk Gelato Recalled by Gelato Boy Due to Undeclared Milk

The Issue: Undeclared Milk

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

Class III — Low RiskOngoing
Refund
FoodJune 12, 2023· Supplement Manufacturing Partner, Inc.

Recalled Item: Havasu Beetroot Powder Recalled by Supplement Manufacturing Partner, Inc....

The Issue: Contains undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 12, 2023· Philips North America

Recalled Item: Ingenia Elition X Magnetic Resonance (MR) system Recalled by Philips North...

The Issue: During installation of the SmokeDetector Interlock, a connecting cable,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2023· Philips North America

Recalled Item: MR 7700 Magnetic Resonance (MR) system Recalled by Philips North America Due...

The Issue: During installation of the SmokeDetector Interlock, a connecting cable,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2023· Philips North America

Recalled Item: Ingenia Elition X Magnetic Resonance (MR) system Recalled by Philips North...

The Issue: The system operator is able to bypass the SmokeDetector Interlock system...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2023· Philips North America

Recalled Item: MR 7700 Magnetic Resonance (MR) system Recalled by Philips North America Due...

The Issue: The system operator is able to bypass the SmokeDetector Interlock system...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2023· Philips North America

Recalled Item: Ingenia Elition S Magnetic Resonance (MR) system Recalled by Philips North...

The Issue: The system operator is able to bypass the SmokeDetector Interlock system...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2023· Philips North America

Recalled Item: Ingenia Elition S Magnetic Resonance (MR) system Recalled by Philips North...

The Issue: During installation of the SmokeDetector Interlock, a connecting cable,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2023· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 7 M20. X-ray Image guided Therapy System. Recalled by PHILIPS...

The Issue: The bolts supporting the FlexMove Carriage may become loose and/or break,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2023· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10 and FD20. X-ray Imaging System. Recalled by PHILIPS MEDICAL...

The Issue: The bolts supporting the FlexMove Carriage may become loose and/or break,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2023· Draeger Medical, Inc.

Recalled Item: Oxylog 3000 Plus emergency and transport ventilator Recalled by Draeger...

The Issue: Draeger has become aware of instances where the device stopped working when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 12, 2023· Abbott

Recalled Item: Abbott Amplatzer Steerable Delivery Sheath (ASDS) Recalled by Abbott Due to...

The Issue: There is an overall reported incidence rate of 0.77% related to observed or...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 12, 2023· Intuitive Surgical, Inc.

Recalled Item: da Vinci Xi/X Tip-Up Fenestrated Grasper Recalled by Intuitive Surgical,...

The Issue: Fenestrated Graspers have a manufacturing issue has the potential to cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2023· Tornier, Inc

Recalled Item: AEQUALIS FLEX REVIVE Assembly Screw 0mm Short Recalled by Tornier, Inc Due...

The Issue: A comingle/swap resulted in the labeling and laser marking on the product to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2023· Tornier, Inc

Recalled Item: AEQUALIS FLEX REVIVE Assembly Screw 0mm Recalled by Tornier, Inc Due to A...

The Issue: A comingle/swap resulted in the labeling and laser marking on the product to...

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

Class II — Potential Health HazardOngoing
FoodJune 9, 2023· Richin Trading Inc

Recalled Item: Sun Wave Brand Jelly Cup (Lychee Flavor) Recalled by Richin Trading Inc Due...

The Issue: Potential choking hazard

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 9, 2023· Richin Trading Inc

Recalled Item: Sun Wave Brand Jelly Cup (Mango Flavor) Recalled by Richin Trading Inc Due...

The Issue: Potential choking hazard

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 9, 2023· Richin Trading Inc

Recalled Item: Sun Wave Brand Jelly Cup (Assorted Flavors) Recalled by Richin Trading Inc...

The Issue: Potential choking hazard

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 8, 2023· Botanas Michoacanas

Recalled Item: Churritos Corn Flour sticks Recalled by Botanas Michoacanas Due to The...

The Issue: The product labels include a Contains statement that did not disclose sesame...

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

Class II — Potential Health HazardOngoing
Refund