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. 3,068 recalls have been distributed to California in the last 12 months.
Showing 2661–2680 of 56,506 recalls
Recalled Item: Broselow Pediatric Emergency Rainbow Tape (distribution by AirLife) Recalled...
The Issue: The impacted tape was manufactured with incorrect information on the tape....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contamac Recalled by Contamac Solutions, Inc. Due to Contact lens insertion...
The Issue: Contact lens insertion solution may lack sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Airsupra (albuterol and budesonide) inhalation aerosol Recalled by...
The Issue: Defective delivery system
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial...
The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog...
The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog...
The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog...
The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FEM-FLEXII Product Name: Femoral Arterial Cannula Model/Catalog...
The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial...
The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFGHANI CORN BREAD "Doda" Recalled by Ariana Sweets Inc. Due to Undeclared...
The Issue: Undeclared allergens (wheat, sesame)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kraft package is labeled as Hummingbird Organic Roasted Salted Cashews...
The Issue: Undeclared hazelnut. The Oregon Trail Mix contains visible hazelnut and was...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Celecoxib Capsules Recalled by AvKARE Due to Presence of Foreign...
The Issue: Presence of Foreign Tablets/Capsules: manufacturer recalled because one...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Esomeprazole Magnesium for Delayed-Release Oral Suspension Recalled by Zydus...
The Issue: Failed Impurities/Degradation Specifications: Out-of-Specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Esomeprazole Magnesium for Delayed-Release Oral Suspension Recalled by Zydus...
The Issue: Failed Impurities/Degradation Specifications: Out-of-Specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SCD Comfort Knee Length Small Recalled by Cardinal Health 200, LLC Due to...
The Issue: Incorrect software logic may cause frequent E1 errors (system high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kendall SCD Blended Comfort Sleeves Knee Length Small - For Recalled by...
The Issue: Incorrect software logic may cause frequent E1 errors (system high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kendall SCD Comfort Sleeves Knee Length Small Recalled by Cardinal Health...
The Issue: Incorrect software logic may cause frequent E1 errors (system high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allon 2001. Part Number: 200-00263 Recalled by Belmont Instrument LLC Due to...
The Issue: An investigation into a report of the patient wrap (ThermoWrap), used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Evolution Upgrade 3.0T Recalled by Philips North America Llc...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia 3.0T CX Recalled by Philips North America Llc Due to...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.