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. 1,763 recalls have been distributed to California in the last 12 months.

56,506 total recalls
1,763 in last 12 months

Showing 1288112900 of 30,923 recalls

Medical DeviceJanuary 17, 2020· Ormco/Sybronendo

Recalled Item: SnapLink Recalled by Ormco/Sybronendo Due to The action is being taken due...

The Issue: The action is being taken due to an increase in complaints relating to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Kentec Medical, Inc

Recalled Item: Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes....

The Issue: Feeding tube plastic tethered closure cap may possibly fracture or break....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Beckman Coulter Inc.

Recalled Item: LabPro Data Management System Recalled by Beckman Coulter Inc. Due to A...

The Issue: A security-only update was released via remote diagnostics on January 14,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Ormco/Sybronendo

Recalled Item: SnapLink Recalled by Ormco/Sybronendo Due to The action is being taken due...

The Issue: The action is being taken due to an increase in complaints relating to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Kentec Medical, Inc

Recalled Item: Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes....

The Issue: Feeding tube plastic tethered closure cap may possibly fracture or break....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Kentec Medical, Inc

Recalled Item: Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes....

The Issue: Feeding tube plastic tethered closure cap may possibly fracture or break....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Kentec Medical, Inc

Recalled Item: Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes....

The Issue: Feeding tube plastic tethered closure cap may possibly fracture or break....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Kentec Medical, Inc

Recalled Item: Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes....

The Issue: Feeding tube plastic tethered closure cap may possibly fracture or break....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Kentec Medical, Inc

Recalled Item: Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes....

The Issue: Feeding tube plastic tethered closure cap may possibly fracture or break....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· COVIDIEN LLC

Recalled Item: Covidien Endo GIA Ultra Universal Stapler 12 mm-intended for resection...

The Issue: Potential for the sterile barrier to be compromised. Products with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2020· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Getinge 46-Series Washer Disinfector Model # 46-4 Recalled by Maquet...

The Issue: Due to a missing water intake for Deionized water on the Getinge 46-Series...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 16, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: COHERENCE Oncologist Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A potential safety issue arises when an offset calculation is followed by a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2020· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Getinge 46-Series Washer Disinfector Model # 46-4 Recalled by Maquet...

The Issue: Due to a missing water intake for Deionized water on the Getinge 46-Series...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 15, 2020· Cardinal Health 200, LLC

Recalled Item: Monoject Hypodermic Safety Needle 30G X 1/2" Item Code 1183005 Recalled by...

The Issue: Non-sterile product was shipped to customers. Product package is labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Cardinal Health 200, LLC

Recalled Item: Monoject Hypodermic Safety Needle 25G x 5/8" Item Code 1182558 Recalled by...

The Issue: Non-sterile product was shipped to customers. Product package is labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Epidural Catheterization Set Recalled by Arrow International...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Epidural Catheterization Kit Recalled by Arrow International...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: Epidural Catheterization Kit with FlexTip Plus Recalled by Arrow...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing