Recalls affecting Florida
Notices that name Florida in their distribution area, plus every nationwide recall — nationwide recalls reach Florida too.
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Class III · 1+ years ago
Philips Ultrasound, Inc VL13-5 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class III · 1+ years ago
Philips Ultrasound, Inc C8-4v Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class III · 1+ years ago
Philips Ultrasound, Inc X5-1 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class II · 1+ years ago
Brand Name: Thor Product Name: NovoThor Gen 3.0 Reg PRX Model/ recall: The potential for a failed welded nut to shear off. When this occurs
The potential for a failed welded nut to shear off. When this occurs, the gas strut on one side of the device becomes detached from the canopy…
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Class III · 1+ years ago
Philips Ultrasound, Inc C10-4ec Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class III · 1+ years ago
Philips Ultrasound, Inc L10-4LAP Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class II · 1+ years ago
Orascoptic Superior Visualization Phantom Nose Pad Accessory Kit 1 pk recall: Due to complaints, loupe nose pads containing nickel may cause an allergic
Due to complaints, loupe nose pads containing nickel may cause an allergic reaction.
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Class III · 1+ years ago
Philips Ultrasound, Inc 7.5MHZ Endo Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class III · 1+ years ago
Philips Ultrasound, Inc L8-4 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class III · 1+ years ago
Philips Ultrasound, Inc SCNHD LA L7-4 HDI Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class III · 1+ years ago
Philips Ultrasound, Inc BP10-5ec Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class III · 1+ years ago
Philips Ultrasound, Inc L12-4 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class III · 1+ years ago
Philips Ultrasound, Inc C9-3v Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class III · 1+ years ago
Philips Ultrasound, Inc X6-1 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class II · 1+ years ago
GE Medical Systems, LLC GE HealthCare OEC 9800 recall: GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k)
GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in certain OEC 9800 and OEC 9900 Elite C-arm Systems. Specifically…
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Class II · 1+ years ago
Baxter Healthcare Corporation Spectrum IQ Infusion Pump, Product Code 3570009 recall: Baxter has identified that certain pumps have potentially been released
Baxter has identified that certain pumps have potentially been released with the grease applied to the cam and motor gears that will break down…
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Class III · 1+ years ago
Philips Ultrasound, Inc C5-2 Lumify Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class III · 1+ years ago
Philips Ultrasound, Inc mC7-2 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class III · 1+ years ago
Philips Ultrasound, Inc C8-5 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class I · 1+ years ago
Medline ReNewal Reprocessed St. Jude Medical Response and Supreme recall: Specific lots of reprocessed electrophysiology catheters may contain small
Specific lots of reprocessed electrophysiology catheters may contain small residual particulates.
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Class III · 1+ years ago
Philips Ultrasound, Inc S9-2 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class I · 1+ years ago
Tandem Diabetes Care, Inc. Battery Operated infusion pumps. t:slim X2 G5 recall: Insulin pumps manufactured with speakers from Revision A and B
Insulin pumps manufactured with speakers from Revision A and B may malfunction ("Malfunction 16") which prevents audible alerts and causes the pumps…
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Class II · 1+ years ago
Zhejiang Luyao Electronics Technology Co., Ltd. Brand Name: Homedics Product Name recall: Regulatory documentation error and misleading color packaging claim
Regulatory documentation error and misleading color packaging claim.
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Class II · 1+ years ago
GE Medical Systems, LLC GE HealthCare OEC 9900 Elite C-arm Systems recall: GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k)
GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in certain OEC 9800 and OEC 9900 Elite C-arm Systems. Specifically…