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 2844128460 of 30,923 recalls

Medical DeviceMay 24, 2013· International Biomedical, Ltd.

Recalled Item: VIA Medical Collection Bag Recalled by International Biomedical, Ltd. Due to...

The Issue: International Biomedical has received reports of interference between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2013· Gyrus Acmi, Incorporated

Recalled Item: GYRUS ACMI Recalled by Gyrus Acmi, Incorporated Due to lack of sterility...

The Issue: lack of sterility assurance

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius Service Replacement 0-Ring. Used in as a service part Recalled by...

The Issue: Incorrect rubber nitrile O-rings distributed instead of the correct material...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2013· SpineFrontier, Inc.

Recalled Item: S-LIFT Inserter Outer Sleeve Product Usage: The Inserter Sleeve is Recalled...

The Issue: The outer sleeve would not fit over the S-LIFT Inserter assembly because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2013· Nidek Inc

Recalled Item: MC-500 Multicolor Laser Photocoagulator using software version 2.20....

The Issue: Retrospective review found that a Engineering Change Order initiated in May...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Prism Medical Services USA

Recalled Item: BC Hammock Mesh Sling (Small) Recalled by Prism Medical Services USA Due to...

The Issue: The product does not meet the firm's size standards, the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Prism Medical Services USA

Recalled Item: BC Hammock Mesh Sling (Large) Recalled by Prism Medical Services USA Due to...

The Issue: The product does not meet the firm's size standards, the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Prism Medical Services USA

Recalled Item: BC Hammock Mesh Sling (Junior) Recalled by Prism Medical Services USA Due to...

The Issue: The product does not meet the firm's size standards, the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Sotera Wireless, Inc.

Recalled Item: ViSi Mobile Chest Sensor (3 lead-wire ECG Recalled by Sotera Wireless, Inc....

The Issue: Sotera Wireless, Inc. is recalling the ViSi Mobile Monitoring System due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-820-000 T4 Zipper Toga (L/XL) Sterile Recalled by...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Zimmer, Inc.

Recalled Item: Bigliani/Flatow¿ The Complete Solution Fukuda Retractors Small Nonsterile...

The Issue: This is a recall expansion from the 2010 recall which now includes seven...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Zimmer, Inc.

Recalled Item: Bigliani/Flatow¿ The Complete Solution Fukuda Retractors Large Nonsterile...

The Issue: This is a recall expansion from the 2010 recall which now includes seven...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Abbott Medical Optics, Inc.

Recalled Item: Sovereign¿ Compact Phacoemulsification System Recalled by Abbott Medical...

The Issue: Abbott Medical Optics Inc. (AMO) initiated this Urgent Notice of Medical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-760-000 T4 Toga Recalled by Stryker Instruments...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-810-000 T4 Zipper Toga (S/M) Sterile Recalled by...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-770-000 T4 Toga Recalled by Stryker Instruments...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments0400-720-000 T4 Pullover Toga (L/XL) Sterile Recalled by...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-840-000 T4 Toga Recalled by Stryker Instruments...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-720-000S5 T5 Pullover Toga w/Peel Away Recalled by...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-820-000S7 T4 XXL Toga w/T3 Cut Recalled by Stryker...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing