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.
Showing 25581–25600 of 56,506 recalls
Recalled Item: On-X Aortic Heart Valve with Anatomic Sewing Ring Product Usage: Recalled by...
The Issue: On-X Valve was mislabeled with the incorrect serial number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAROLINA(R) LIQUID CHEMISTRIES CORP. ETHA RGT. KIT Recalled by Carolina...
The Issue: Supplier testing showed that the absorbance rate of the Ethyl Alcohol Assay...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipid Panel test strips Recalled by Polymer Technology Systems, Inc. Due to...
The Issue: Some lots of test strips do not fit tightly into the optical block, and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences(R) IntraClude(TM) Intra-Aortic Occlusion Device is a...
The Issue: Edwards Lifesciences has received a limited number of customer reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CHOL+HDL+GLU test strips Recalled by Polymer Technology Systems, Inc. Due to...
The Issue: Some lots of test strips do not fit tightly into the optical block, and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAROLINA(R) LIQUID CHEMISTRIES CORP. ETHA RGT. KIT Recalled by Carolina...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipid Panel test strips (as a component of smart bundles) Recalled by...
The Issue: Some lots of test strips do not fit tightly into the optical block, and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NORepinephrine 16 mg added to 0.9% Sodium Chloride (PF) Recalled by KRS...
The Issue: Labeling: Label mix-up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine 4 mg added to 5% Dextrose 250 mL Bag (PF) Recalled by KRS...
The Issue: Labeling: Label mix-up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: infants* IBUPROFEN Recalled by Tris Pharma Inc. Due to Superpotent Drug:...
The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Infants' Ibuprofen Recalled by Tris Pharma Inc. Due to Superpotent Drug:...
The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ezetimibe and Simvastatin Tablets 10mg/80 mg Recalled by Dr. Reddy's...
The Issue: Presence of Foreign Substance: Product complaint of black speckles observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Infants' Ibuprofen Recalled by Tris Pharma Inc. Due to Superpotent Drug:...
The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluocinolone Acetonide Topical Solution Recalled by LUPIN SOMERSET Due to...
The Issue: Failed Impurities/Degradation Specifications: Expansion of October 2018...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fujifilm FDR Go PLUS Recalled by Fujifilm Medical Systems U.S.A., Inc. Due...
The Issue: FUJIFILM Medical Systems U.S.A., Inc., Modality Systems became aware of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proximal Humerus Plate Recalled by Miami Device Solutions, LLC. Due to Right...
The Issue: Right Proximal Humerus Plates. Product component parts MDS130108R, may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ottogi Ppushu Ppushu Grilled Chicken Flavor 3.17oz x 40ea Item Recalled by...
The Issue: Undeclared allergen; egg.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ottogi Ppushu Ppushu BBQ Flavor 3.17oz x 40ea Item #21503007 Recalled by...
The Issue: Undeclared allergen; egg.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ottogi Spicy Seafood flavor Udon Odongtong 5PK 1lb 5.16oz x Recalled by...
The Issue: Undeclared allergen; egg.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ottogi Ramen Sari (Extra Noodle) 3.88oz x 48ea Item #21101009 Recalled by...
The Issue: Undeclared allergen; egg.
Recommended Action: Do not consume. Return to store for a refund or discard.