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. 2,856 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,856 in last 12 months

Showing 2258122600 of 56,506 recalls

Medical DeviceSeptember 18, 2019· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: XCELA Recalled by Angiodynamics Inc. (Navilyst Medical Inc.) Due to Snap...

The Issue: Snap lock connectors provided within implantable port kits may not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2019· Biomedical Polymers, Inc.

Recalled Item: Manual Diff Dropper Recalled by Biomedical Polymers, Inc. Due to The metal...

The Issue: The metal cannula of the device either broke and the broken piece left in...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 18, 2019· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: BIOFLO 8F SINGLE PLASTIC FILLED Recalled by Angiodynamics Inc. (Navilyst...

The Issue: Snap lock connectors provided within implantable port kits may not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2019· Senseonics, Inc.

Recalled Item: Eversense CGM SENSOR (FG-4200-00-301)-Continuous Glucose Monitor Recalled by...

The Issue: Eversense Sensors have prematurely stopped functioning due to inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2019· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: BIOFLO 8F SINGLE TITANIUM NON- FILLED Recalled by Angiodynamics Inc....

The Issue: Snap lock connectors provided within implantable port kits may not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2019· GN Hearing A/S

Recalled Item: Behind-the-Ear hearing aids Recalled by GN Hearing A/S Due to GN Hearing...

The Issue: GN Hearing received reports from our manufacturing site in US regarding a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2019· Medline Industries Inc

Recalled Item: EVENCARE G3 Blood Glucose Test Strips Recalled by Medline Industries Inc Due...

The Issue: Incomplete seal and premature expiration of individually packaged Blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2019· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the Recalled by...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2019· GN Hearing A/S

Recalled Item: In-the-Ear hearing aids Recalled by GN Hearing A/S Due to GN Hearing...

The Issue: GN Hearing received reports from our manufacturing site in US regarding a...

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

Class II — Potential Health HazardOngoing
FoodSeptember 18, 2019· Wismettac Asian Foods, INC

Recalled Item: Shirakiku Buckwheat Noodles Yamaimo Soba With Concentration Soup Base...

The Issue: Product label identifies bonito, but product dipping sauce actually contains...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 18, 2019· Avella of Deer Valley, Inc. Store 38

Recalled Item: Povidone Iodine Recalled by Avella of Deer Valley, Inc. Store 38 Due to Lack...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 18, 2019· GCP Laboratories Inc

Recalled Item: Major Infants' Gas Relief Drops Recalled by GCP Laboratories Inc Due to...

The Issue: Microbial Contamination of Non-Sterile Product.

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2019· Akorn, Inc.

Recalled Item: Lidocaine Hydroclhoride Jelly USP Recalled by Akorn, Inc. Due to cGMP...

The Issue: cGMP Deviations: firm reported finding metal particulate matter in the...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 17, 2019· Huy Fong Foods, Inc

Recalled Item: Siracha HOT Chili Sauce Net Wt. 28 oz. (1 lb. 12 oz.) (793 g) Recalled by...

The Issue: Firm received complaint of Siracha sauce bulging at top seal and exploding...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 17, 2019· Cook Inc.

Recalled Item: Pneumothorax Tray Recalled by Cook Inc. Due to Lidstock perforation line may...

The Issue: Lidstock perforation line may be over the sterile area of the tray, when it...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Abbott Gmbh & Co. KG

Recalled Item: Alinity ci Level Sensor Recalled by Abbott Gmbh & Co. KG Due to Potential...

The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Abbott Gmbh & Co. KG

Recalled Item: Accessory kit Recalled by Abbott Gmbh & Co. KG Due to Potential reliability...

The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· GE Healthcare, LLC

Recalled Item: CardioLab/ComboLab Recording Systems Recalled by GE Healthcare, LLC Due to...

The Issue: Potential for failure of the patient leakage current test. There is a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Axis-Shield Diagnostics, Ltd.

Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...

The Issue: There is a potential performance issue as detected by an under-recovery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Abbott Gmbh & Co. KG

Recalled Item: Accessory kit Recalled by Abbott Gmbh & Co. KG Due to Potential reliability...

The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...

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

Class II — Potential Health HazardOngoing