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. 2,799 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,799 in last 12 months

Showing 3682136840 of 56,506 recalls

DrugJune 27, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: Carvediol Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJune 24, 2016· Teva North America

Recalled Item: Amoxicillin for Oral Suspension USP Recalled by Teva North America Due to...

The Issue: Superpotent drug: Out of specification test result for assay during...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 24, 2016· Baxter Healthcare Corp.

Recalled Item: Synovis VASCU-GUARD Peripheral Vascular Patch in the following sizes and...

The Issue: Baxter is issuing a safety alert in response to postmarketing reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2016· Cook Inc.

Recalled Item: Roadrunner Uniglide Hydrophilic Wire Guide Recalled by Cook Inc. Due to...

The Issue: Potential coating contamination with glass particles.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 24, 2016· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD Trucount Tubes: Catalog number: 340334 Hematology: BD Trucount tubes...

The Issue: One lot of BD Trucount Absolute Counting Tubes (IVD) may not be sealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2016· Moller Vital

Recalled Item: Molift Air 205 Recalled by Moller Vital Due to Potential for the bolt on the...

The Issue: Potential for the bolt on the suspension coupling on the Molift Air to come...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 2.3MM Tapered Router Recalled by Stryker Instruments Div. of Stryker...

The Issue: A variation in flute depth on the routers was observed. The variation in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2016· The Anspach Effort, Inc.

Recalled Item: Light Adaptor for Small Battery Drive and Small Battery Drive II. Recalled...

The Issue: There was a potential for the Adaptor and Light Adaptor for Small Battery...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 24, 2016· The Anspach Effort, Inc.

Recalled Item: Adaptor for Small Battery Drive and Small Battery Drive II. Recalled by The...

The Issue: There was a potential for the Adaptor and Light Adaptor for Small Battery...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 24, 2016· PerkinElmer, Inc

Recalled Item: Perkin Elmer RoboRack 25ul Recalled by PerkinElmer, Inc Due to Filter Tips...

The Issue: Filter Tips molded incorrectly and may not seal to the Varispan tip adaptor...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Olympus Corporation of the Americas

Recalled Item: OER-Pro Endoscope Reprocessor Recalled by Olympus Corporation of the...

The Issue: New warning requiring Users to conduct duodenoscope precleaning and manual...

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

Class II — Potential Health HazardOngoing
DrugJune 23, 2016· Hospira Inc.

Recalled Item: Diazepam Injection USP 10mg/2mL (5 mg/mL Recalled by Hospira Inc. Due to...

The Issue: Crystallization: Product contains particulate identified to be crystallized...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 23, 2016· Mondelez International

Recalled Item: Nabisco Honey Maid Teddy Grahams Cinnamon Cubs Graham Snacks Net Recalled by...

The Issue: Teddy Graham Cub Snacks were produced using Grain Craft Flour containing...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 23, 2016· Inner Health Group, Inc dba Michael's Naturopathic Programs

Recalled Item: Michael's Naturopathic Programs Cholesterol Metabolism Factors 270 count...

The Issue: May contain undeclared milk (in the form of calcium caseinate) and soy.

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 23, 2016· Prime Time International

Recalled Item: PRIME TIME Cucumbers Recalled by Prime Time International Due to Potential...

The Issue: Sun and Sands Enterprise dba Prime Time International is recalling cucumber...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 23, 2016· Varian Medical Systems, Inc.

Recalled Item: Optical Surface Monitoring System{Align RT Plus} This is used on Recalled by...

The Issue: Varian Medical Systems has received reports that unintended changes were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· The Metrix Company

Recalled Item: Dual Chamber Container fill with gravity/attached transfer sets Recalled by...

The Issue: An issue was identified after a redesign of the auto compounding device. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· The Metrix Company

Recalled Item: Container fill and transfer sets Recalled by The Metrix Company Due to An...

The Issue: An issue was identified after a redesign of the auto compounding device. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· The Metrix Company

Recalled Item: Container fill and transfer sets Recalled by The Metrix Company Due to An...

The Issue: An issue was identified after a redesign of the auto compounding device. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· The Metrix Company

Recalled Item: AUTOCOMP6 XP High Speed Compounder Recalled by The Metrix Company Due to An...

The Issue: An issue was identified after a redesign of the auto compounding device. The...

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

Class II — Potential Health HazardOngoing