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. 2,866 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,866 in last 12 months

Showing 1008110100 of 30,686 recalls

Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2021· RanD S.r.l.

Recalled Item: Hang&Go (kit for hyperthermic perfusion) Recalled by RanD S.r.l. Due to The...

The Issue: The sterilization contractor informed the company of a quality issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2021· RanD S.r.l.

Recalled Item: Ch24 round silicone catheter Recalled by RanD S.r.l. Due to The...

The Issue: The sterilization contractor informed the company of a quality issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2021· Sentinel CH SpA

Recalled Item: ACE Control Set - IVD Control set for the quantitative Recalled by Sentinel...

The Issue: Claim for stability after reconstitution from lyophilized to liquid form...

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

Class III — Low RiskOngoing
Medical DeviceApril 30, 2021· Nico Corp.

Recalled Item: Myriad-LX Light Source-for delivery of light to the surgical field Recalled...

The Issue: (1) Updated IFU for the LX Illumination Packs: Warning - Avoid contact...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2021· Nico Corp.

Recalled Item: NICO Myriad-LX Illumination Pack: Mvriad-LX Illumination Pack. 11ga Recalled...

The Issue: (1) Updated IFU for the LX Illumination Packs: Warning - Avoid contact...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2021· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Synapse Cardiovascular (Synapse CV). Software Versions: 6.0 to 6.2.1 The...

The Issue: Software versions 6.0.4 to 6.2.1 using Advanced Reporting -possibility that...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Exact Medical Manufacturing, Inc.

Recalled Item: Hays Ultrasound kit Item ID: H1000SE Recalled by Exact Medical...

The Issue: No 510k for the product to be used in a natural or surgical opening to the body

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Exact Medical Manufacturing, Inc.

Recalled Item: Probe Cover Recalled by Exact Medical Manufacturing, Inc. Due to No 510k for...

The Issue: No 510k for the product to be used in a natural or surgical opening to the body

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Exact Medical Manufacturing, Inc.

Recalled Item: 6" x 48" Elastic Poly Probe Cover Recalled by Exact Medical Manufacturing,...

The Issue: No 510k for the product to be used in a natural or surgical opening to the body

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Exact Medical Manufacturing, Inc.

Recalled Item: Probe Cover Recalled by Exact Medical Manufacturing, Inc. Due to No 510k for...

The Issue: No 510k for the product to be used in a natural or surgical opening to the body

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Exact Medical Manufacturing, Inc.

Recalled Item: Probe Cover Elastic Poly 6" x 48"- Ultrasonic Transducer Cover Recalled by...

The Issue: No 510k for the product to be used in a natural or surgical opening to the body

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Exact Medical Manufacturing, Inc.

Recalled Item: Probe Cover Recalled by Exact Medical Manufacturing, Inc. Due to No 510k for...

The Issue: No 510k for the product to be used in a natural or surgical opening to the body

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Exact Medical Manufacturing, Inc.

Recalled Item: Probe Cover Recalled by Exact Medical Manufacturing, Inc. Due to No 510k for...

The Issue: No 510k for the product to be used in a natural or surgical opening to the body

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Exact Medical Manufacturing, Inc.

Recalled Item: Probe Cover 6" x 48" regular PE w/ 2 Elastic Recalled by Exact Medical...

The Issue: No 510k for the product to be used in a natural or surgical opening to the body

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Exact Medical Manufacturing, Inc.

Recalled Item: Probe Cover Recalled by Exact Medical Manufacturing, Inc. Due to No 510k for...

The Issue: No 510k for the product to be used in a natural or surgical opening to the body

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

Class II — Potential Health HazardOngoing