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. 3,040 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,040 in last 12 months

Showing 61016120 of 30,923 recalls

Medical DeviceJuly 19, 2023· IHB OPERATIONS B.V.

Recalled Item: Freedom Boom models series: F110 Recalled by IHB OPERATIONS B.V. Due to...

The Issue: Weakened connection point on the adjustable suspension arm, potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2023· Philips Medical Systems Nederland B.V.

Recalled Item: Allura Xper series Recalled by Philips Medical Systems Nederland B.V. Due to...

The Issue: A foot switch pedal may get stuck in the active position when the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2023· Philips Medical Systems Nederland B.V.

Recalled Item: Azurion Recalled by Philips Medical Systems Nederland B.V. Due to A foot...

The Issue: A foot switch pedal may get stuck in the active position when the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2023· Philips Medical Systems Nederland B.V.

Recalled Item: MultiDiagnost-Eleva Recalled by Philips Medical Systems Nederland B.V. Due...

The Issue: A foot switch pedal may get stuck in the active position when the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2023· Randox Laboratories Ltd.

Recalled Item: Randox Liquid Protein Calibrators-SP CAL-(LIQ)-In vitro diagnostic product...

The Issue: As part of the firm's ongoing quality monitoring (see internal complaint #...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2023· Preat Corp

Recalled Item: Preat Recalled by Preat Corp Due to The healing abutments contain a...

The Issue: The healing abutments contain a dimensional condition that may lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2023· Preat Corp

Recalled Item: Preat Recalled by Preat Corp Due to The healing abutments contain a...

The Issue: The healing abutments contain a dimensional condition that may lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2023· Preat Corp

Recalled Item: Preat Recalled by Preat Corp Due to The healing abutments contain a...

The Issue: The healing abutments contain a dimensional condition that may lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2023· Abbott Medical

Recalled Item: Proclaim" XR 7 Implantable Pulse Generator (previously known Recalled by...

The Issue: Firm has received complaints from patients who are unable to exit MRI...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2023· Abbott Medical

Recalled Item: Proclaim Plus 5 Implantable Pulse Generator Product Description: Recalled by...

The Issue: Firm has received complaints from patients who are unable to exit MRI...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2023· Abbott Medical

Recalled Item: Proclaim XR 5 Implantable Pulse Genterator (previously known Recalled by...

The Issue: Firm has received complaints from patients who are unable to exit MRI...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2023· Abbott Medical

Recalled Item: Infinity 5 Implantable Pulse Generator Product Description: The Recalled by...

The Issue: Firm has received complaints from patients who are unable to exit MRI...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2023· Abbott Medical

Recalled Item: Infinity 7 Implantable Pulse Generator Product Description: The Recalled by...

The Issue: Firm has received complaints from patients who are unable to exit MRI...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2023· Abbott Medical

Recalled Item: Proclaim DRG Implantable Pulse Generator Product Description: The Recalled...

The Issue: Firm has received complaints from patients who are unable to exit MRI...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2023· Abbott Medical

Recalled Item: Proclaim Plus 7 Implantable Pulse Generator Product Description: Recalled by...

The Issue: Firm has received complaints from patients who are unable to exit MRI...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2023· Smiths Medical ASD Inc.

Recalled Item: PORTEX 0.5u HYDROPHOBIC DISC FILTER Recalled by Smiths Medical ASD Inc. Due...

The Issue: Smiths Medical identified a labeling error in which the barcode (UDI) was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2023· WOM World Of Medicine AG

Recalled Item: Aquilex Fluid Control System-Intended to provide fluid distension of the...

The Issue: The display of inflow volume can reach its limit of 30,000 ml during long...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2023· RAYSEARCH LABORATORIES AB

Recalled Item: RayCare software Recalled by RAYSEARCH LABORATORIES AB Due to An issue was...

The Issue: An issue was found in Software RayCare 5A, 5B, 6A, including service packs,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2023· Peter Lazic Gmbh

Recalled Item: L-Aneurysm Clip TITANIUM Paddle-Clip Recalled by Peter Lazic Gmbh Due to...

The Issue: Wrong product coloring. The paddle clips should be blank, but they are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2023· Peter Lazic Gmbh

Recalled Item: L-Aneurysm Clip TITANIUM Paddle-Clip Recalled by Peter Lazic Gmbh Due to...

The Issue: Wrong product coloring. The paddle clips should be blank, but they are...

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

Class II — Potential Health HazardOngoing