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. 2,851 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,851 in last 12 months

Showing 2484124860 of 56,506 recalls

Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1)Solero...

The Issue: Updated Warning Statements in the Operator's Manual/Directions for Use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2019· Zimmer Surgical Inc

Recalled Item: Zimmer Biomet Alvarado Knee Holder Base Plate Assembly and Foot Piece...

The Issue: Foreign Material in the Alvarado Knee Holder Base Plate Assembly and Foot...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2019· Ad-Tech Medical Instrument Corporation

Recalled Item: AD-TECH Spencer Probe Depth Electrode Product Usage: The Ad-Tech Depth...

The Issue: An Ad-Tech Clinical Specialist, attended a case on April 15, 2019. During...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2019· Med Tec Inc

Recalled Item: CIVCO Solstice(TM) SRS Immobilization System Recalled by Med Tec Inc Due to...

The Issue: There is a potential for movement of the Solstice Tilting Head Fixation...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2019· Abbott Gmbh & Co. KG

Recalled Item: Alinity c Cuvette Segments Recalled by Abbott Gmbh & Co. KG Due to...

The Issue: Individual cuvettes within the Alinity c Cuvette Segment may become seated...

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

Class II — Potential Health HazardOngoing
FoodApril 15, 2019· Jensen Tuna Inc

Recalled Item: Frozen ground tuna Recalled by Jensen Tuna Inc Due to Potential Salmonella...

The Issue: Potential to be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 14, 2019· Schreiber Foods Inc

Recalled Item: Shredded and blocks of Colby & Monterey Jack cheese - Recalled by Schreiber...

The Issue: Product is being recalled due to the presence of foreign material (hard...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 14, 2019· Schreiber Foods Inc

Recalled Item: Great Value Recalled by Schreiber Foods Inc Due to Foreign Object Contamination

The Issue: Product is being recalled due to the presence of foreign material (hard...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 12, 2019· TIDI PRODUCTS

Recalled Item: Posey Connected Twice-As-Tough Cuffs Recalled by TIDI PRODUCTS Due to Not...

The Issue: Not meeting design specifications.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2019· Geistlich Pharma North America, Inc.

Recalled Item: Geistlich Bio-Oss Pen Recalled by Geistlich Pharma North America, Inc. Due...

The Issue: When unscrewing the green cap from the pen, a visible piece of green plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2019· Geistlich Pharma North America, Inc.

Recalled Item: Geistlich Bio-Oss Pen Recalled by Geistlich Pharma North America, Inc. Due...

The Issue: When unscrewing the green cap from the pen, a visible piece of green plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2019· Tecan US, Inc.

Recalled Item: Freedom EVO 200 - Product Usage: It is intended for routine laboratory tasks...

The Issue: Gas springs not always replaced within the interval specified.

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

Class II — Potential Health HazardOngoing