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. 3,047 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,047 in last 12 months

Showing 51815200 of 30,923 recalls

Medical DeviceDecember 21, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE BLOOD CULTURE COLLECTION KIT Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· Ivoclar Vivadent, Inc.

Recalled Item: Article No. NA6050411 Recalled by Ivoclar Vivadent, Inc. Due to Affected...

The Issue: Affected product may not perform as expected; the amalgam powder may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· Paragon 28, Inc.

Recalled Item: Phantom TTC Nail Recalled by Paragon 28, Inc. Due to Medical devices...

The Issue: Medical devices distributed, prior to sterilization

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· AMD Medicom Inc.

Recalled Item: HENRY SCHEIN¿ CRITERION¿ EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-2448)...

The Issue: Level 3 masks were produced on alternate non-validated production equipment...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2023· Barco N.V.

Recalled Item: Barco MDSC-8527 NXF Recalled by Barco N.V. Due to Barco became aware of a...

The Issue: Barco became aware of a problem with I2C cables in the manufacturing process...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2023· CooperSurgical, Inc.

Recalled Item: global Medium Recalled by CooperSurgical, Inc. Due to The firm has become...

The Issue: The firm has become aware of a sudden increase in complaints for three...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2023· Zyno Medical LLC

Recalled Item: Zyno Medical Z800 Large Volume Infusion Pumps -Intended to provide Recalled...

The Issue: When utlizing the patient query feature on the Zyno Medical Z-800WF pumps...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2023· OriGen Biomedical, Inc.

Recalled Item: Accessory Sets Syringes: 6ml syringe with a female luer with Recalled by...

The Issue: Accessory sets contain a syringes not yet qualified for the accessory's...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2023· Acumed LLC

Recalled Item: Acu-Loc and Acu-Loc 2 bone plates Recalled by Acumed LLC Due to Distribution...

The Issue: Distribution without Pre-Market Clearance

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2023· Smiths Medical ASD Inc.

Recalled Item: smiths medical Medfusion Model 4000 syringe pump Recalled by Smiths Medical...

The Issue: Medfusion Model 4000 syringe infusion pumps, with the following software...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 18, 2023· Vortex Surgical Inc.

Recalled Item: Vortex Surgical ACTU8 FORCEPS Recalled by Vortex Surgical Inc. Due to Reason...

The Issue: Reason for the voluntary recall is residue was identified on the two forceps...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2023· St. Jude Medical, Atrial Fibrillation Division, Inc.

Recalled Item: TactiFlex Ablation Sensor Enabled Ablation Catheter Recalled by St. Jude...

The Issue: When the catheters are used with the EnSiteX EP System, the system does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2023· Philips North America

Recalled Item: BrightView XCT Recalled by Philips North America Due to Detector may...

The Issue: Detector may unexpectedly fall due to a component failure. If the detector...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Total immunoglobulin M (IgM total) IVD Recalled by Siemens Healthcare...

The Issue: Potential for a negative bias with quality control (QC) and patient sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2023· Olympus Corporation of the Americas

Recalled Item: ESG PK CUTTING FORCEPS Recalled by Olympus Corporation of the Americas Due...

The Issue: The jaw may fracture prior to the procedure during the inspection instructed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2023· Philips North America

Recalled Item: ProxiDiagnost upgrade- A Multi-functional general Radiography and...

The Issue: Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2023· Philips North America

Recalled Item: ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy...

The Issue: Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2023· Globus Medical, Inc.

Recalled Item: ExcelsiusGPS Cannula A Recalled by Globus Medical, Inc. Due to Devices may...

The Issue: Devices may not be rendered sterile due to an internal gap that may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2023· Philips North America

Recalled Item: BrightView Recalled by Philips North America Due to Detector may...

The Issue: Detector may unexpectedly fall due to a component failure. If the detector...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2023· Philips North America

Recalled Item: BrightView X Recalled by Philips North America Due to Detector may...

The Issue: Detector may unexpectedly fall due to a component failure. If the detector...

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

Class I — Serious Health HazardOngoing