Hobbs Medical recalls

Hobbs Medical has 73 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 27 Nov 2024. 72 are still ongoing.

Total recalls73since 2018
Last 12 months0reported
Class I00% of total
Ongoing72latest 27 Nov 2024

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 73 100%Class III 0 0%

Why hobbs medical is recalled

By year

Ongoing hobbs medical recalls

72 active
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIPosi-Stop Injection Needle recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIPosi-Stop Injection Needle recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIPosi-Stop Injection Needle recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIPosi-Stop Injection Needle recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIPosi-Stop Injection Needle recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIPosi-Stop Injection Needle recalled by Hobbs MedicalHobbs MedicalOtherNationwide

All hobbs medical recalls, newest first

73 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIPosi-Stop Injection Needle recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIPosi-Stop Injection Needle recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIPosi-Stop Injection Needle recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIPosi-Stop Injection Needle recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIPosi-Stop Injection Needle recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIPosi-Stop Injection Needle recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIPosi-Stop Injection Needle recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIPosi-Stop Injection Needle recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIPosi-Stop Injection Needle recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIHobbs Biliary Pigtail Stent Kits (containing 3412) recalledHobbs MedicalOtherNationwide
DeviceCLASS IIFreeman Pancreatic Flexi-Stent recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIHobbs Posi-Stop Injection Needle recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIPolypectomy Snare recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIFlex-Ez Guide Wire Disposable For endoscopy procedures recalledHobbs MedicalOtherNationwide
DeviceCLASS IIHobbs Biliary Pigtail Stent Kits (containing 6105) recalledHobbs MedicalOtherNationwide
DeviceCLASS IIFreeman Pancreatic Flexi-Stent Kits: Single Pigtail recalledHobbs MedicalOtherNationwide
DeviceCLASS IIHobbs Posi-Stop Injection Needle recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIHobbs Biliary Pigtail Stent Kits recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIHobbs Helical Retrieval Basket recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIHobbs Biliary Pigtail Stent Kits (containing 3412) recalledHobbs MedicalOtherNationwide
DeviceCLASS IIPolypectomy Snare recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIHobbs Scope Introducer recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIFreeman Pancreatic Flexi-Stent recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIHobbs Biliary Pigtail Stent Kits (containing 3412) recalledHobbs MedicalOtherNationwide
DeviceCLASS IIFreeman Pancreatic Flexi-Stent Kit recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIFreeman Pancreatic Flexi-Stent Kit recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIPolypectomy Snare recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIHobbs Retrieval Forceps recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIHobbs Helical Retrieval Basket recalled by Hobbs MedicalHobbs MedicalOtherNationwide
DeviceCLASS IIFreeman Pancreatic Flexi-Stent recalled by Hobbs MedicalHobbs MedicalOtherNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.