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. 3,026 recalls have been distributed to California in the last 12 months.
Showing 9021–9040 of 56,506 recalls
Recalled Item: Unguentine Ointment Recalled by Ecometics, Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: YAGER'S LINIMENT (Camphor and Turpentine Oil) 3.1% and 8.12% respectively...
The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Proboscis/Piston Assembly Recalled by Ortho-Clinical Diagnostics, Inc. Due...
The Issue: Ortho Clinical Diagnostics (QuidelOrtho) confirmed certain Proboscis/Piston...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soft Serve on the Go brand Razzle n' Dazzle Peanut Butter flavor Recalled by...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Soft Serve on the Go brand Caramel Vanilla flavor Recalled by Real Kosher...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Butter Flavored Popcorn Naturally & Artificially Flavored Recalled by...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Soft Serve on the Go brand Vanilla Chocolate flavor Recalled by Real Kosher...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Soft Zero on the Go brand Lite Peanut Butter flavor Recalled by Real Kosher...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Soft Serve on the Go brand Sorbet Strawberry Mango Sorbet flavor Recalled by...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Centered Glenosphere w/Screw Recalled by FX SHOULDER Due to Centered...
The Issue: Centered glenosphere box may contain an eccentric glenosphere.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3ML Syringe Luer Lock with needle 20GX1 Recalled by Fresenius Medical Care...
The Issue: There is a potential for blood backfill leakage and foreign material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10ML SYRINGE LUER LOCK W/NEEDLE Recalled by Fresenius Medical Care Holdings,...
The Issue: There is a potential for blood backfill leakage and foreign material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10ML SYRINGE LUER LOCK W/OUT NEEDLE Recalled by Fresenius Medical Care...
The Issue: There is a potential for blood backfill leakage and foreign material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Iron_2 (IRON_2) Reagents Recalled by Siemens Healthcare...
The Issue: There is a potential for a positive bias on Quality Control (QC) and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prucka 3 Amplifiers Recalled by GE Medical Systems Information Technologies...
The Issue: A diode on the power supply of the Prucka 3 Amplifier used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oculus Pentacam AXL Recalled by Oculus Optikgeraete GMBH Due to Their is a...
The Issue: Their is a potential that optical devices with insufficient anti- coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oculus Myopia Master Recalled by Oculus Optikgeraete GMBH Due to Their is a...
The Issue: Their is a potential that optical devices with insufficient anti- coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oculus Pentacam AXL Wave Recalled by Oculus Optikgeraete GMBH Due to Their...
The Issue: Their is a potential that optical devices with insufficient anti- coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PLUVICTO 1 Recalled by Advanced Accelerator Applications USA, Inc. Due to...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: vials were labeled with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heartmate 3 LVAS Implant Kit Recalled by Thoratec Corp. Due to Inability to...
The Issue: Inability to start and/or complete the coring procedure due to inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.