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. 2,811 recalls have been distributed to California in the last 12 months.
Showing 34621–34640 of 56,506 recalls
Recalled Item: Alaska Salmon Bites (jerky) Recalled by Authentic Alaska Due to Undeclared Soy
The Issue: Alaska Salmon Bites (jerky), Rhubarb & Raspberries flavor is recalled due to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Maquet Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optilite IgG4 Kit Product Code: LK009.OPT.A Recalled by The Binding Site...
The Issue: A change to the lower end of the measuring range and product insert did not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Express Dry Seal Suction OCEAN DRAIN Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOSAVE Hybrid IABP and CARDIOSAVE Rescue IABP affected part number...
The Issue: Maquet has received 3 confirmed complaints related to the Li-lon Battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: The intended use listed in the English and localized language IFUs for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Express Dry Seal Suction OASIS DRAIN Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Express Dry Seal Suction OCEAN DRAIN Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X upgraded to XCT 882454 Recalled by Philips Medical Systems...
The Issue: The intended use listed in the English and localized language IFUs for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Oasis Dry Suction Water Seal Chest Drain Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Express Dry Seal Suction Chest Drain Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FlowSmart Set MiniMed Pro-set Rx Only Distributed by Medtronic Recalled...
The Issue: Patients are reporting high blood glucose (HBG) levels while using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oncentra External Beam Oncentra Brachy Product Usage: Oncentra is radiation...
The Issue: Cross profile for Varian 60 degree wedge shows "horns."
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX Cardiovascular The IMPAX CV Reporting module consists of a Recalled by...
The Issue: A customer experienced when using IMPAX CV Reporting software, specifically,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAKO RIO THA Application User Guides Recalled by Mako Surgical Corporation...
The Issue: Five (5) AFMEA Risk Control Measures are missing from the MAKO RIO THA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Keyspan High-High Speed USB to Serial Adapter Product Usage: The Recalled by...
The Issue: Power outages causes reporting software to shutdown.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venlafaxine Hydrochloride extended release capsules Recalled by Aurobindo...
The Issue: Failed Tablet/Capsule Specifications: Some bottles contain punctured, and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TEMAZEPAM CAPSULES USP Recalled by Vintage Pharmaceuticals LLC, DBA...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Furosemide Tablets USP Recalled by Roxane Laboratories, Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: An unusually thick tablet was reported...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.