Product Recalls in Florida
Product recalls affecting Florida — including food, drugs, consumer products, medical devices, and vehicles distributed to Florida. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,830 recalls have been distributed to Florida in the last 12 months.
Showing 42001–42020 of 55,837 recalls
Recalled Item: Azithromycin tablets Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zonisamide capsules Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine besylate tablets Recalled by American Health Packaging Due to...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clarithromycin tablets Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril tablets Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine besylate tablets Recalled by American Health Packaging Due to...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril tablets Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Famotidine tablets Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine besylate tablets Recalled by American Health Packaging Due to...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azithromycin tablets Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Praeger's California Veggie Burgers Gluten Free 11 oz. Manufactured...
The Issue: Dr. Praeger's Gluten Free California Burgers contain undeclared soy.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Schiller PB 1000 Recalled by Merge Healthcare, Inc. Due to Non-invasive...
The Issue: Non-invasive blood pressure pumps (NIBP) voltage is not sufficient and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinite 200 PRO in vitro diagnostic. Product Usage: The Tecan Recalled by...
The Issue: A firmware bug causes incorrect values to be displayed for specific measured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELI 380 Electrocardiograph. The ELI 380 is intended to be a high-performance...
The Issue: Mortara Instrument, Inc. has recently become aware of a potential safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 540. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinite 200 in vitro diagnostic. Product Usage: The Tecan Infinite Recalled...
The Issue: A firmware bug causes incorrect values to be displayed for specific measured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima IGS 320. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova 3100IQ. Angiographic X-ray systems used in generating...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 520. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiation Therapy Treatment Planning System software RayStation is a...
The Issue: An error caused by a floating point precision problem tends to cause a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.