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. 2,839 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,839 in last 12 months

Showing 2822128240 of 56,506 recalls

DrugJune 27, 2018· Aidarex Pharmaceuticals LLC

Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...

The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2018· Aidarex Pharmaceuticals LLC

Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...

The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2018· Aidarex Pharmaceuticals LLC

Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...

The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 27, 2018· Genicon, Inc.

Recalled Item: Genicon EZee Single Use Specimen Retrieval Bag - Product Usage: Recalled by...

The Issue: Genicon is providing updated IFU labeling to users to provide clarity on how...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Elekta Instrument AB

Recalled Item: Leksell GammaPlan 11.1 Product Usage: Leksell GammaPlan is a computer-based...

The Issue: The margin tool in Leksell GammaPlan 11.1 systematically overestimates...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· bioMerieux, Inc.

Recalled Item: BACT/ALERT VIRTUO system Recalled by bioMerieux, Inc. Due to The BACT/ALERT...

The Issue: The BACT/ALERT VIRTUO Instrument Firmware version R2.0 allows relocation of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· bioMerieux, Inc.

Recalled Item: BACT/ALERT VIRTUO system Recalled by bioMerieux, Inc. Due to The BACT/ALERT...

The Issue: The BACT/ALERT VIRTUO Instrument Firmware version R2.0 allows relocation of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· bioMerieux, Inc.

Recalled Item: BACT/ALERT VIRTUO system Recalled by bioMerieux, Inc. Due to The BACT/ALERT...

The Issue: The BACT/ALERT VIRTUO Instrument Firmware version R2.0 allows relocation of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Recalled by Philips Medical Systems Gmbh, DMC Due to The...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: BuckyDiagnost Ceiling System (Stitching Patient Support) 704031 Recalled by...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Dual Detector (Stitching Patient Support) 712022 Recalled by...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: EasyDiagnost Eleva DRF (Stitching Patient Support) 706032 Recalled by...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Single Detector (Stitching Patient Support) 712020 Recalled...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028 Recalled...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026 Recalled by...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4.1 Flex / Value (Stitching Patient Support) 712028 Recalled...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4 High Performance (Stitching Patient Support) 712027...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Release 3 (Stitching Patient Support) 712025 Recalled by...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712081 Recalled by...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing