Product Recalls in Vermont
Product recalls affecting Vermont — including food, drugs, consumer products, medical devices, and vehicles distributed to Vermont. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,541 recalls have been distributed to Vermont in the last 12 months.
Showing 3041–3060 of 27,157 recalls
Recalled Item: MEDLINE OPEN HEART Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Medline Industries, LP. has identified certain kits containing the recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE OPEN HEART PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Medline Industries, LP. has identified certain kits containing the recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE HEART CABG CDS Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Medline Industries, LP. has identified certain kits containing the recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Access TSH (3rd IS) assay is a paramagnetic particle Recalled by Beckman...
The Issue: Certain lots of Access TSH reagent packs may produce erroneously low TSH...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE HEART OVERHEAD TABLE PACK Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Medline Industries, LP. has identified certain kits containing the recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE OPEN HEART NIMC KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Medline Industries, LP. has identified certain kits containing the recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Sterile Laparoscopy Pack Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: CONMED Corporation (vendor) initiated a recall for select lot numbers of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAWK Advanced Hypothermia Management Set Recalled by Safeguard US Operating...
The Issue: Incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAWK Warming Grid Recalled by Safeguard US Operating LLC Due to Incorrect...
The Issue: Incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kits of Convenience containing 1 of the 2 Item Numbers: Recalled by...
The Issue: Incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: NOVA ORTHO-MED INC. Product Name: MONARCH ROLLATOR BLUE Recalled...
The Issue: Firm identified a potential risk for a fall hazard. When the end user is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: NOVA ORTHO-MED INC. Product Name: MONARCH ROLLATOR RED Recalled...
The Issue: Firm identified a potential risk for a fall hazard. When the end user is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FastPack TSH Calibrator Kit Recalled by Qualigen Inc Due to Thyroid...
The Issue: Thyroid Stimulating Hormone (TSH) calibrator card has an incorrect barcode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: NOVA ORTHO-MED INC. Product Name: MONARCH ROLLATOR PURPLE...
The Issue: Firm identified a potential risk for a fall hazard. When the end user is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Endoscopic Flushing Pump Recalled by Olympus Corporation of the...
The Issue: During product testing, Olympus identified an intermittent loss of function...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVS Anchor-C Cervical Cage System Instructions For Use (IFU)- eIFU Recalled...
The Issue: Labeling Correction: Instructions For Use (IFU)-Updated electronic Rev 5,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KINOVA Jaco assistive robot. Model Numbers: PJ 0000 0001 Recalled by Kinova...
The Issue: Potential installation issue that could result in a fire hazard in the event...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StealthStation S8 App versions 1.3.0 and 1.3.2 Recalled by Medtronic...
The Issue: Due to two software anomalies that can occur within a spine procedure. Two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Healgen Series Reagent strips for Urinalysis are composed of several...
The Issue: The reason for this recall is Healgen Scientific Ltd. has determined that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Code Name: 722282 Azurion 7 M20 722281 Azurion 5 Recalled by PHILIPS...
The Issue: Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.