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. 2,683 recalls have been distributed to Florida in the last 12 months.
Showing 36721–36740 of 55,837 recalls
Recalled Item: Invacare Precise Rx Pediatric Flowmeter Model Number: IRCPF16 AW. Packed...
The Issue: The rear gradation scale was screen printed upside down on the flowmeter gauge.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: lnvacare Precise Rx Pediatric Flowmeter Model Number: IRCPF16. Packed one...
The Issue: The rear gradation scale was screen printed upside down on the flowmeter gauge.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Al Rasheed Sardine Item #4017 Label not available - NYSDAM sampling....
The Issue: Greenland Trading Corporation is recalling Al Rasheed Sardines due to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PoleStar system (N20 / N30) Warning Lamps Control Box Recalled by Medtronic...
The Issue: Medtronic Navigation is recalling certain components of the PoleStar system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Image1 SPIES X-LINK Camera Control Unit (CCU) Recalled by Karl Storz...
The Issue: Potential electrical interference issue when the Image1 SPIES X-LINK and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARGATROBAN Injection in 0.9% Sodium Chloride 250 mg/250 mL (1 mg/mL)...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Linezolid Injection 600 mg/300 mL Rx Only Recalled by Teva North America Due...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eptifibatide Injection 75 mg/100 mL (0.75 mg/mL) single use vial Recalled by...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ondansetron Injection USP 40 mg/20 mL (2 mg/mL) Recalled by Teva North...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fresh Express Kit Caesar salad Recalled by Fresh Express Incorpated Due to...
The Issue: The condiment kits in some Caesar Salad bags contain undeclared allergens:...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Earnest Eats Chewy Granola Dark Chocolate Almond .2 Recalled by Annona...
The Issue: Potential Listeria monocytogenes contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Achillon Minimally Invasive Device for Achilles Tendon Rupture Treatment The...
The Issue: Data from internal studies suggests there may be a potential that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System Recalled by Elekta, Inc. Due to It is...
The Issue: It is possible that that the selected Plan-of-the Day could be accidently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ Chemistry (Syva Onboard) Theophylline_2 (THEO_2) Reagent is for in...
The Issue: Siemens Healthcare Diagnostics has confirmed the Syva¿ EMIT¿ 2000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syva¿ EMIT¿ 2000 Theophylline - Catalog # 4P019UL /SMN#10445324 is Recalled...
The Issue: Siemens Healthcare Diagnostics has confirmed the Syva¿ EMIT¿ 2000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB Sciex API 3200MD" LC/MS/MS System. In-Vitro Diagnostic Instrument Part...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB SCIEX QTRAP¿ 4500MD LC/MS/MS System Mass Spectrometer for In-Vitro...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB SCIEX 3200MD QTRAP¿ LC/MS/MS System Mass Spectrometer for In-Vitro...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB SCIEX Triple Quad 4500MD LC/MS/MS System. Mass Spectrometer for Recalled...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Inc., Cardiac Rhythm and Heart Failure Due...
The Issue: This Pacing Lead System does not comply with Section 8.5.2.3 of IEC 60601-1,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.