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.

56,506 total recalls
2,839 in last 12 months

Showing 2578125800 of 56,506 recalls

Medical DeviceDecember 21, 2018· Draeger Medical, Inc.

Recalled Item: VentStar Basic 250 Recalled by Draeger Medical, Inc. Due to Incorrectly...

The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 21, 2018· Draeger Medical, Inc.

Recalled Item: ID Circuit Watertrap (P) 180 Recalled by Draeger Medical, Inc. Due to...

The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 21, 2018· Draeger Medical, Inc.

Recalled Item: VentStar Basic (P) 250 Recalled by Draeger Medical, Inc. Due to Incorrectly...

The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 21, 2018· Draeger Medical, Inc.

Recalled Item: VentStar Basic 180 Recalled by Draeger Medical, Inc. Due to Incorrectly...

The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 21, 2018· Draeger Medical, Inc.

Recalled Item: VentStar Basic (P) 180 Recalled by Draeger Medical, Inc. Due to Incorrectly...

The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 21, 2018· Draeger Medical, Inc.

Recalled Item: ID Circuit Basic 250 Recalled by Draeger Medical, Inc. Due to Incorrectly...

The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 21, 2018· Draeger Medical, Inc.

Recalled Item: VentStar Anesthesia WT(P) 180 Recalled by Draeger Medical, Inc. Due to...

The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...

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

Class I — Serious Health HazardOngoing
DrugDecember 20, 2018· Torrent Pharma Inc.

Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2018· Torrent Pharma Inc.

Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2018· Torrent Pharma Inc.

Recalled Item: LOSARTAN POTASSIUM and HYDROCHLOROTHIAZIDE TABLETS Recalled by Torrent...

The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2018· Torrent Pharma Inc.

Recalled Item: LOSARTAN POTASSIUM and HYDROCHLOROTHIAZIDE TABLETS Recalled by Torrent...

The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2018· Torrent Pharma Inc.

Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2018· Lupin Pharmaceuticals Inc.

Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: Presence of Particulate Matter: Product complaints received of grey flecks,...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 20, 2018· Akorn Inc

Recalled Item: COSOPT Ophthalmic Solution Recalled by Akorn Inc Due to Failed Stability...

The Issue: Failed Stability Specifications: out of specification results for...

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

Class III — Low RiskOngoing
Refund
DrugDecember 20, 2018· Lupin Pharmaceuticals Inc.

Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: Presence of Particulate Matter: Product complaints received of grey flecks,...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 20, 2018· Lupin Pharmaceuticals Inc.

Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: Presence of Particulate Matter: Product complaints received of grey flecks,...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 20, 2018· Lupin Pharmaceuticals Inc.

Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: Presence of Particulate Matter: Product complaints received of grey flecks,...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 20, 2018· Funky Chunky LLC

Recalled Item: Nutty Choco Pop Recalled by Funky Chunky LLC Due to Nutty Choco Pop has in...

The Issue: Nutty Choco Pop has in incorrect label and does not declare that it contains...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 20, 2018· Steris Corporation

Recalled Item: AMSCO 5000 Series Washer/Disinfector Model # 5052 Recalled by Steris...

The Issue: The software in the systems may not process the cycle originally intended....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2018· Steris Corporation

Recalled Item: AMSCO 3000 Series Washer/Disinfector Model # 3052 Recalled by Steris...

The Issue: The software in the systems may not process the cycle originally intended....

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

Class II — Potential Health HazardOngoing