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. 1,095 recalls have been distributed to California in the last 12 months.

56,506 total recalls
1,095 in last 12 months

Showing 28181–28200 of 56,506 recalls

DrugJuly 5, 2018· Teva Pharmaceuticals USA

Recalled Item: Fluocinolone Acetonide Topical Solution Recalled by Teva Pharmaceuticals USA...

The Issue: Failed Impurities and Degradation Specifications and Subpotent Drug:...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 3, 2018· Medgyn Products, Inc.

Recalled Item: Monsel's Solution (Ferric Subsulfate) Recalled by Medgyn Products, Inc. Due...

The Issue: CGMP Deviations: The manufacturer of this product recalled because they were...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 3, 2018· Radiometer America Inc

Recalled Item: ABL800 analyzer Recalled by Radiometer America Inc Due to The analyzer...

The Issue: The analyzer software may cause a mis-match of patient demographics and test...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2018· Arrow International Inc

Recalled Item: Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip...

The Issue: One lot of product is from product code AK-22502 so it contains a 2-lumen, 5...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2018· Alden Optical

Recalled Item: Zenlens Toric-Gas Permeable Contact lenses for Daily Wear in a Recalled by...

The Issue: Vials labeled for the prescriptions contained incorrect lenses

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2018· Alden Optical

Recalled Item: Zen RC Toric-Gas permeable contact lenses for Daily Wear in Recalled by...

The Issue: Vials labeled for the prescriptions contained incorrect lenses

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2018· Abbott Vascular

Recalled Item: PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended Recalled...

The Issue: Incorrect expiration being entered for one lot.

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

Class II — Potential Health HazardOngoing
FoodJuly 3, 2018· Byrd Cookie Co

Recalled Item: PINK LEMONADE COOKIES Byrd's FAMOUS COOKIES Recalled by Byrd Cookie Co Due...

The Issue: Red 40 & Red 3 were not listed in the ingredients statement

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 3, 2018· ConvaTec, Inc

Recalled Item: AbViser AutoValve IAP (intra- abdominal pressure) Monitoring Device Recalled...

The Issue: Bubble Leak Testing on AbViser AutoValve IAP Monitoring Devices without...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2018· Water Pik, Inc.

Recalled Item: Waterpik Sonic-Fusion Professional Recalled by Water Pik, Inc. Due to...

The Issue: Charging base may overheat with localized melting and sparking, possibly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2018· Cypress Medical Products LLC

Recalled Item: Powder Free Vinyl Exam Gloves Recalled by Cypress Medical Products LLC Due...

The Issue: The firm is recalling one lot of McKesson Powder Free Vinyl Exam Gloves...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2018· Hudson Scientific LLC

Recalled Item: iTOVi Tracker/Scanner Recalled by Hudson Scientific LLC Due to The device...

The Issue: The device and its accessories may not have been manufactured according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2018· Radiometer America Inc

Recalled Item: Product: ABL800 FLEX with Crea. The ABL800 with Crea is Recalled by...

The Issue: From three incidents in Denmark and Sweden, comparison studies on patient...

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

Class II — Potential Health HazardOngoing
DrugJuly 2, 2018· AuroMedics Pharma LLC

Recalled Item: Piperacillin and Tazobactam for Injection USP 3.375 grams per vial Recalled...

The Issue: Presence of Particulate Matter: identified as glass and silicone material

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 29, 2018· Fagron Compounding Services LLC dba Fagron Sterile Services

Recalled Item: Neostigmine Methylsulfate Injection Solution Recalled by Fagron Compounding...

The Issue: Labeling: Label Error on Declared Strength: syringes of Neostigmine...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 29, 2018· Fagron Compounding Services LLC dba Fagron Sterile Services

Recalled Item: Neostigmine Methylsulfate Injection Solution Recalled by Fagron Compounding...

The Issue: Labeling: Label Error on Declared Strength: syringes of Neostigmine...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1600 Analyzer (SMN 11066000). The Atellica" Solution is Recalled...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: 3D TOP Ceiling Stand Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: In rare cases of insufficient maintenance or high clinical workload, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica Sample Handler Prime (SMN 11069001). The Atellica" Solution is...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: 3D V Recalled by Siemens Medical Solutions USA, Inc Due to In rare cases of...

The Issue: In rare cases of insufficient maintenance or high clinical workload, the...

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

Class II — Potential Health HazardOngoing