Recall archive
5 recalls · page 1 of 1
Reported Nov 27, 2024
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4720
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hobbs Medical, Inc.
Matched: Brand — Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the…
8 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 19, 2022
Hobbs Medical Spray Catheter: The Mistifier: 2.6mm 260cm Disposable For endoscopy procedures Ref: 2190
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hobbs Medical, Inc.
Matched: Brand · Product · Product details — Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from…
60 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 27, 2022
Hobbs Medical Polypectomy Snare, Catalog No. 7202
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hobbs Medical, Inc.
Matched: Brand · Product · Product details — During use, the sheath of the device may accordion at the proximal end where the sheath meets the shrink band. Kinking of the sheath may prevent the…
FDA (openFDA device enforcement)
Reported Mar 9, 2022
Bronchial Microbiology Brush, Catalog Number 4310 and 4320. Microbial sampling is performed by compressing a spring as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hobbs Medical, Inc.
Matched: Brand — The labeling for the Microbiology Brush identifies the device as a Bronchial Microbiology Brush. The device is only cleared for gastrointestinal use…
FDA (openFDA device enforcement)
Reported Jun 13, 2018
Hobbs Bronchial Cytology Brushes, Model Number 4202; 4204; 4206 To be utilized by a trained physician and/or trained…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hobbs Medical, Inc.
Matched: Brand · Product · Product details — Device was marketed for uses outside the 510(k) clearance.
FDA (openFDA device enforcement)
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