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. 2,696 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,696 in last 12 months

Showing 3968139700 of 56,506 recalls

DrugDecember 17, 2015· Bio-pharm, Inc.

Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution Recalled by Bio-pharm, Inc. Due...

The Issue: Failed Impurities/Degradation Specifications: Product recalled due to...

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

Class III — Low RiskOngoing
Refund
FoodDecember 17, 2015· Swinomish Fish Company, Inc

Recalled Item: Native Catch Salmon Bacon Recalled by Swinomish Fish Company, Inc Due to...

The Issue: Traditional flavor of Native Catch Salmon Bacon product is recalled because...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 17, 2015· Swinomish Fish Company, Inc

Recalled Item: Native Catch Salmon Bacon Recalled by Swinomish Fish Company, Inc Due to...

The Issue: Peppered flavor of Native Catch Salmon Bacon product is recalled because it...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 17, 2015· Mars Chocolate North America

Recalled Item: Dove Chocolate Assortment Snowflakes Net. Wt. 24.0 oz. Distributed by...

The Issue: Dove Chocolate Assortment Snowflakes may contain undeclared peanuts, what...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 17, 2015· Arthrex, Inc.

Recalled Item: Arthrex IBalance TKA Tibial Tray Size 2 - Catalog # AR-503-TTTC Recalled by...

The Issue: Devices reported to have a smooth texture to the outer surface of the metal,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView are gamma cameras Recalled by Philips Medical Systems (Cleveland)...

The Issue: The firm discovered four issues with the BrightView Family systems. Issue 1:...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT & BrightView XCT Upgrade Recalled by Philips Medical Systems...

The Issue: The firm discovered four issues with the BrightView Family systems. Issue 1:...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView X are gamma cameras Recalled by Philips Medical Systems...

The Issue: The firm discovered four issues with the BrightView Family systems. Issue 1:...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2015· Merge Healthcare, Inc.

Recalled Item: RadSuite Recalled by Merge Healthcare, Inc. Due to Potential incorrect...

The Issue: Potential incorrect Standardized Uptake Values (SUV) measurements in RadSuite.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2015· Stryker Sustainability Solutions

Recalled Item: Reprocessed Stryker Color Cuff and Color Cuff II Adult Tourniquet Recalled...

The Issue: Reprocessed Stryker Pressure Tourniquet Cuffs were mislabeled, including...

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

Class II — Potential Health HazardOngoing
FoodDecember 16, 2015· Ocean Group Inc.

Recalled Item: Masago Lake Smelt Roe 6 oz. Code:4866010101 Recalled by Ocean Group Inc. Due...

The Issue: Product contains undeclared soy and wheat.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 16, 2015· Twinings North America, Inc.

Recalled Item: TWININGS OF London ENGLISH BREAKFAST BLACK TEA DECAFFEINATED Recalled by...

The Issue: Twinings English Breakfast Black Tea 12ct Kcups, were packaged in cartons...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 16, 2015· GE Inspection Technologies, LP

Recalled Item: GE Inspection Technologies Recalled by GE Inspection Technologies, LP Due to...

The Issue: GE Inspection Technologies, LP ("GE") has discovered that certain of its...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2015· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: Cardiosave Hybrid and rescue IABP Recalled by Maquet Datascope Corp -...

The Issue: Maquet has recieved information that in some Cardiosave IABPS, the scroll...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2015· Stryker Spine

Recalled Item: AccuLIF PL Tubing Set and AccuLIF TL Tubing Set AccuLIF Recalled by Stryker...

The Issue: There were two potential interference conditions identified with the way the...

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

Class II — Potential Health HazardOngoing
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: SlimeX-15 Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: Asset BOLD Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: Oasis Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: Ultimate Formula Capsules Recalled by Bee Extremely Amazed LLC Due to...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: SLIM TRIM U Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund