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. 2,723 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,723 in last 12 months

Showing 2548125500 of 55,837 recalls

DrugJanuary 10, 2019· McGuff Compounding Pharmacy Services, Inc.

Recalled Item: Lipoic Acid Injection (aka Alpha Lipoic Acid or Thioctic Acid) Recalled by...

The Issue: Presence of Particulate Matter: filmy/cloudy particulate observed in vial.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2019· MAJOR PHARMACEUTICALS

Recalled Item: Losartan Potassium Tablets Recalled by MAJOR PHARMACEUTICALS Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 10, 2019· PerkinElmer Life and Analytical Sciences, Wallac, OY

Recalled Item: AutoDELFIA¿ hCG Kit Recalled by PerkinElmer Life and Analytical Sciences,...

The Issue: hCG analyte concentrations may be decreased up to 15- 20% at the lower...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· PerkinElmer Life and Analytical Sciences, Wallac, OY

Recalled Item: AutoDELFIA¿ hCG Kit Recalled by PerkinElmer Life and Analytical Sciences,...

The Issue: hCG analyte concentrations may be decreased up to 15- 20% at the lower...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· Arrow International Inc

Recalled Item: Arrow¿ Two-Lumen Central Venous Catheterization Set with Blue FlexTip¿...

The Issue: The product lidstock contains a labelling error. The lidstock states the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· Ottobock Orthopedic Industrie

Recalled Item: 21Y15 MagValve Product Usage: The PushValves/ MagValves is intended...

The Issue: Some of the installed valve-inserts have a diameter smaller than the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· Ottobock Orthopedic Industrie

Recalled Item: 21Y14 PushValve Product Usage: The PushValves/ MagValves is intended...

The Issue: Some of the installed valve-inserts have a diameter smaller than the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· Bio-Rad Laboratories, Inc

Recalled Item: EVOLIS Microplate System (Catalog no. 89700) with TimeLiner Data Management...

The Issue: User-induced circumstances can contribute to the EVOLIS Microplate Processor...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· PerkinElmer Life and Analytical Sciences, Wallac, OY

Recalled Item: DELFIA¿ hCG Kit Recalled by PerkinElmer Life and Analytical Sciences,...

The Issue: hCG analyte concentrations may be decreased up to 15- 20% at the lower...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· Ottobock Orthopedic Industrie

Recalled Item: 21Y14=S PushValve upper part Product Usage: The PushValves/ MagValves is...

The Issue: Some of the installed valve-inserts have a diameter smaller than the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· Arrow International Inc

Recalled Item: Arrow¿ Two-Lumen Central Venous Catheterization Kit with Blue FlexTip¿...

The Issue: The product lidstock contains a labelling error. The lidstock states the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· ConvaTec, Inc

Recalled Item: Forceps Blue Recalled by ConvaTec, Inc Due to An internal assessment of...

The Issue: An internal assessment of packaging confirmed the potential for a breach in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC50 Government Bundle Recalled by Philips North America, LLC Due...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· ConvaTec, Inc

Recalled Item: Nelaton Urinary Catheter Recalled by ConvaTec, Inc Due to An internal...

The Issue: An internal assessment of packaging confirmed the potential for a breach in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· ConvaTec, Inc

Recalled Item: FilterFlow Suction Handle CH24 Recalled by ConvaTec, Inc Due to An internal...

The Issue: An internal assessment of packaging confirmed the potential for a breach in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC70 w/o trolley Government Bundle Recalled by Philips North...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC70 w/trolley Government Bundle Recalled by Philips North...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC30 w/ trolley Government Bundle Recalled by Philips North...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC30 w/o trolley Government Bundle Recalled by Philips North...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· ConvaTec, Inc

Recalled Item: Feeding Tube Metric Recalled by ConvaTec, Inc Due to An internal assessment...

The Issue: An internal assessment of packaging confirmed the potential for a breach in...

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

Class II — Potential Health HazardOngoing