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. 2,867 recalls have been distributed to California in the last 12 months.
Showing 21681–21700 of 30,923 recalls
Recalled Item: Flexichamber Anti-Static Valved Collapsible Holding Chamber Recalled by FSC...
The Issue: Product had torn/loose seal around the mouthpiece.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Item # 4042-CPR Rescue Kit Recalled by Lifeline First Aid LLC Due to First...
The Issue: First aid kits or rescue kits are recalled because they contains the CPR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen Laboratory Automation System Recalled by Ortho-Clinical Diagnostics...
The Issue: If the user selects the Comment or Interpretation option (in the enGEN .gsb...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Saw Sagittal Catalog Number: ES 300 Recalled by Medtronic Sofamor Danek Usa,...
The Issue: Medtronic Powered Surgical Solutions testing of the Sagittal Saw Rocker Arm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COSEAL Surgical Sealant Kit Recalled by Baxter Healthcare Corp Due to...
The Issue: Potential for incomplete dissolution of the polyethylene glycol (PEG)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COSEAL Surgical Sealant Kit Recalled by Baxter Healthcare Corp Due to...
The Issue: Potential for incomplete dissolution of the polyethylene glycol (PEG)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris System PC Unit Model 8015 with software versions 9.17 and 9.19...
The Issue: A patient weight can be populated incorrectly under certain conditions when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COSEAL Surgical Sealant Kit Recalled by Baxter Healthcare Corp Due to...
The Issue: Potential for incomplete dissolution of the polyethylene glycol (PEG)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norian Drillable Inject 5 CC-Sterile Recalled by Synthes (USA) Products LLC...
The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Trabecular Metal Tibia Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Zimmer Inc. is initiating a recall of specific Persona" Trabecular Metal"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norian Drillable Inject 10 CC-Sterile Recalled by Synthes (USA) Products LLC...
The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norian Drillable Inject 3 CC-Sterile Recalled by Synthes (USA) Products LLC...
The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hettich Centrifuge Modules: StreamLAB Centrifuge Module (10372372 or...
The Issue: Premature bucket failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Pump RF Patient Cassette Recalled by Medical Vision Ab Due to...
The Issue: Sterility of device may be compromised due to sterile package breakage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piccolo Composite Tibia and Femoral Nailing Systems - Ball Tip Recalled by...
The Issue: Firm received complaints where the Piccolo Composite Ball Tip Guide Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIOOA I (EP I84) Rabbit Monoclonal Antibody Recalled by Cell Marque...
The Issue: Cell Marque became aware of some lots of SIOOA I (EP I84) Rabbit Monoclonal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm Synapse PACS software version 4.4.000 Recalled by Fujifilm Medical...
The Issue: Synapse cannot display image files, DICOM SR files, and/or Annotation files....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Revolution CT The system is intended for head Recalled by GE Healthcare,...
The Issue: GEHC has become aware of a potential safety issue in the Revolution CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products AFP Reagent Pack Recalled by ORTHO-CLINICAL...
The Issue: Ortho Clinical Diagnostics (OCD) confirmed that specific lots of VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Histoplasma Yeast Complement Fixation Antigen Dilute Ref# H30150 The fungal...
The Issue: The device was found to have bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.