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. 1,020 recalls have been distributed to California in the last 12 months.

56,506 total recalls
1,020 in last 12 months

Showing 43421–43440 of 56,506 recalls

Medical DeviceMarch 26, 2015· Handicare USA, Inc.

Recalled Item: ReTurn belt Recalled by Handicare USA, Inc. Due to Complaints were received...

The Issue: Complaints were received that the heat-welded seam on the wipeable belt's...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Olympus America Inc.

Recalled Item: EVIS EXERA II Duodenovideoscope OLYMPUS TJF TypeQ180V. This instrument has...

The Issue: New and validated reprocessing procedures have been issued for the Olympus...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· PhotoMedex, Inc.

Recalled Item: Iamin Moist Dressing and the Iamin Hydrating Gel: intended to Recalled by...

The Issue: The labeling for the Iamin family of medical devices (e.g. printed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 3/16 in. Trocar with Single Drain Curved Trocar with Wound Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 1/8 in. Curved Trocar with Wound Drain Curved Trocar with Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 3/16 in. Round Drain with Trocar Curved Trocar with Wound Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 1/4 in. Round Drain with Trocar Curved Trocar with Wound Recalled by Stryker...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Ambulating Bulb Ambulating Bulb: The Ambulating Bulb comprises four main...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Diamedix Corporation

Recalled Item: Diamedix Is-CMV IgG Test Kit Recalled by Diamedix Corporation Due to Product...

The Issue: Product contained an incorrect substrate.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 1/4 in. Trocar with Single Drain Curved Trocar with Wound Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 1/4 in. Double Trocar with Wound Drain Curved Trocar with Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
DrugMarch 26, 2015· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Fexofenadine Hydrochloride Tablets Recalled by Mylan Institutional, Inc....

The Issue: Failed Impurities/Degradation Specifications: the manufacturer, recalled...

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

Class III — Low RiskOngoing
Refund
DrugMarch 26, 2015· Actavis Laboratories, FL, Inc.

Recalled Item: Cartia XT (diltiazem HCl extended-release capsules Recalled by Actavis...

The Issue: Presence of Foreign Substance; fine residue or dust identified as aluminum...

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

Class III — Low RiskOngoing
Refund
FoodMarch 26, 2015· Mead Johnson Nutrition

Recalled Item: Pregestimil ready to use 20 calorie Recalled by Mead Johnson Nutrition Due...

The Issue: Some Pregestimil 20 Calorie Nursette Bottles from batch EV5A6F were...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 25, 2015· Laax, Inc.

Recalled Item: TIGERPAW System II Recalled by Laax, Inc. Due to Increase of field reports...

The Issue: Increase of field reports involving issues with the TIGERPAW System II...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 25, 2015· Lumenis Limited

Recalled Item: Light Sheer Desire Diode Laser System with XC Handpiece Accessory options....

The Issue: Device software treatment preset parameters for the XC treatment handpiece...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2015· Nidek Inc

Recalled Item: Dual Delivery 4DD-1 of GYC-1000 Green Laser Photocoagulator system GYC4DD-1:...

The Issue: Accessories to the GYC-1000 laser were missing Laser Aperture labels.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2015· Nidek Inc

Recalled Item: Endophotocoagulation Delivery 4EP-1 of GYC-1000 Green Laser Photocoagulator...

The Issue: Accessories to the GYC-1000 laser were missing Laser Aperture labels.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2015· Laax, Inc.

Recalled Item: TIGERPAW System II Recalled by Laax, Inc. Due to Increase of field reports...

The Issue: Increase of field reports involving issues with the TIGERPAW System II...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 25, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Universal Charger Product Usage: The Stryker Universal Battery Charger is...

The Issue: The Stryker Universal Battery Charger is not transmitting usage data to the...

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

Class III — Low RiskOngoing