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. 1,638 recalls have been distributed to Vermont in the last 12 months.
Showing 46121–46140 of 47,027 recalls
Recalled Item: AMPHOTERICIN B OPHTHALMIC (0.5ML Recalled by Franck's Lab Inc., d.b.a....
The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIMIX 30MG / 4MG INJECTABLE 10 ML Recalled by Franck's Lab Inc., d.b.a....
The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AMIKACIN P. F. 250MG/ML INJECTABLE 2 ML Recalled by Franck's Lab Inc.,...
The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUPIVACAINE/LIDOCAINE 0.11% / 0.44% INJECTABLE 150 ML (1 PRODUCT) Recalled...
The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYALURONIDASE / LIDOCAINE / BUPICAVAINE 7.1U/9.5MG/3.5MG/ML INJECTABLE 210...
The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FORMIX 100MCG / 30MG / 1MG INJECTABLE 10 ML Recalled by Franck's Lab Inc.,...
The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CEFAZOLIN IN ARTIFICIAL TEARS 50MG/ML OPHTHALMIC 10 ML Recalled by Franck's...
The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUPIVACAINE/HYDROMORPHONE Recalled by Franck's Lab Inc., d.b.a. Franck's...
The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AMINOPHYLLINE 20ML Recalled by Franck's Lab Inc., d.b.a. Franck's...
The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROMORPHONE/BACLOFEN/BUPIVACAINE (0.9% NACL) 50MG/1000MCG/7.5MG/ML...
The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EDETATE DISODIUM PF IN BSS 3% OPHTHALMIC 10 ML Recalled by Franck's Lab...
The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of inaccurate Scale factor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Advantage Workstations Recalled by GE Healthcare, LLC Due to...
The Issue: GE Healthcare is informing you of incorrect measurements when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Seno Advantage 1.x Recalled by GE Healthcare, LLC Due to GE Healthcare...
The Issue: GE Healthcare has become aware of an issue associated with the magnification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Advantage CT/PET Fusion for Advantage Windows Workstation with Volume...
The Issue: GE Healthcare has become aware of a potential safety issue due to incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra(TM) Jarit(R) Take-Apart Endoscopic Instruments. Integra(TM) Jarit(R)...
The Issue: The Integra(TM) Jarit(R) Take-Apart Laparoscopic Instrument shafts were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA Esophageal Intubation Detector (EID) Recalled by LMA North America Inc...
The Issue: The recall was initiated because LMANA has received a complaint that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace Portal software and Extended Brillance Workspace software...
The Issue: The Intellispace Portal software and Extended Brillance Workspace software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bipolar Forceps model number: S02-XXX Recalled by Stingray Surgical...
The Issue: On 05/23/2012, Stingray Surgical Products, LLC., Boca Raton, FL initiated a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intellispace Portal software. Intellispace Portal is a multimodality thin...
The Issue: Philips is issuing a software update to the Intellispace Portal systems to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.