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. 2,799 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,799 in last 12 months

Showing 3618136200 of 56,506 recalls

Medical DeviceAugust 24, 2016· Azer Scientific, Inc.

Recalled Item: Glucose Tolerance Beverage- Orange 50 gram Concentration Recalled by Azer...

The Issue: Out of Specification Microbiological test results

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Azer Scientific, Inc.

Recalled Item: Fruit Punch Glucose Recalled by Azer Scientific, Inc. Due to Out of...

The Issue: Out of Specification Microbiological test results

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: SIEMENS IMMULITE/IMMULITE 2000 Systems Rubella IgM (RUM) Recalled by Siemens...

The Issue: Siemens received multiple customer complaints indicating an increase in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: SIEMENS IMMULITE/IMMULITE 1000 Systems Rubella IgM (RUM) Recalled by Siemens...

The Issue: Siemens received multiple customer complaints indicating an increase in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Philips Medical Systems

Recalled Item: Ingenuity Core Model Number 728321 Product Usage: Computed Tomography X-ray...

The Issue: The infant performance test did not meet the test specification for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Philips Medical Systems

Recalled Item: Ingenuity CT Model Number 728326 Product Usage: Computed Tomography X-ray...

The Issue: The infant performance test did not meet the test specification for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Baxter Corporation Englewood

Recalled Item: 0.2 Micron Filter Recalled by Baxter Corporation Englewood Due to Baxter...

The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for all...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 24, 2016· Philips Medical Systems

Recalled Item: Brilliance 64 CT Model Number 728231 Product Usage: Computed Tomography...

The Issue: The infant performance test did not meet the test specification for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Philips Medical Systems

Recalled Item: Ingenuity Core 128 Model Number 728323 Product Usage: Computed Tomography...

The Issue: The infant performance test did not meet the test specification for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· R & D Systems, Inc.

Recalled Item: R&D Systems Recalled by R & D Systems, Inc. Due to R&D Systems, Inc....

The Issue: R&D Systems, Inc. received two customer complaints that results of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Integra LifeSciences Corp. d.b.a. Integra Pain Management

Recalled Item: PHS Spinal Tray 24G Gertie Marx Recalled by Integra LifeSciences Corp....

The Issue: Integra LifeSciences has recently identified that one lot of Spinal Tray 24...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Integra LifeSciences Corp. d.b.a. Integra Pain Management

Recalled Item: Integra Cranial Access Kits Recalled by Integra LifeSciences Corp. d.b.a....

The Issue: Integra LifeSciences has been notified of a medical device recall by...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Teleflex Medical

Recalled Item: WECK¿ Horizon" Manual-Load Ligating Clip Applier Recalled by Teleflex...

The Issue: Misbranded: Incorrect etching on the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2016· Integra LifeSciences Corp.

Recalled Item: Integral Lumbar Drainage Set Recalled by Integra LifeSciences Corp. Due to...

The Issue: During final sampling inspection, one of the lots was discovered with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2016· Integra LifeSciences Corp.

Recalled Item: Integra Ventricular Catheter Accessory Kit Recalled by Integra LifeSciences...

The Issue: During final sampling inspection, one of the lots was discovered with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2016· Integra LifeSciences Corp.

Recalled Item: Integra Drainage Accessory Kits Recalled by Integra LifeSciences Corp. Due...

The Issue: During final sampling inspection, one of the lots was discovered with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2016· Integra LifeSciences Corp.

Recalled Item: Integra Straight Ventricular Catheter F8 Recalled by Integra LifeSciences...

The Issue: During final sampling inspection, one of the lots was discovered with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2016· Integra LifeSciences Corp.

Recalled Item: CUSA Dissectron Fingertip Laparoscopic Cannula Recalled by Integra...

The Issue: During final sampling inspection, one of the lots was discovered with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2016· Integra LifeSciences Corp.

Recalled Item: Integra Lumbar Drainage Set Recalled by Integra LifeSciences Corp. Due to...

The Issue: During final sampling inspection, one of the lots was discovered with a...

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

Class II — Potential Health HazardOngoing
DrugAugust 22, 2016· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund