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. 2,322 recalls have been distributed to Vermont in the last 12 months.
Showing 31281–31300 of 47,027 recalls
Recalled Item: Spirit Plus Bed Recalled by CHG Hospital Beds Inc Due to Stryker Medical is...
The Issue: Stryker Medical is initiating a voluntary recall of the Spirit Select and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to Wire in...
The Issue: Wire in tubing can become exposed, posing potential harm to the intubated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DULOXETINE Delayed-Release Capsules Recalled by Golden State Medical Supply...
The Issue: Labeling; Incorrect or Missing Lot and/or Exp Date; incorrect expiration...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvediol Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvediol Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvediol Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended Release Tablets USP (SR) 150 mg Rx Recalled...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvediol Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CORE¿ Suction Irrigation Handpiece without Probe for Single Solution or...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Suction Irrigation Handpiece Y-Tubing set Recalled by ConMed...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Trumpet Handpiece with 5mm x 32cm Length Probe Recalled by ConMed...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The 9025TRU Arterial Blood Gas (ABG) Kit is used to Recalled by Cardinal...
The Issue: Arterial Blood Gas (ABG) Kit- Missing Safety Component. The ABG Kit(s) have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Suction Irrigation Handpiece without Probe for Single Solution Bags...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Trumpet Handpiece only Recalled by ConMed Corporation Due to The...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe Recalled by...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe Recalled by...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.3MM Tapered Router Recalled by Stryker Instruments Div. of Stryker...
The Issue: A variation in flute depth on the routers was observed. The variation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner Uniglide Hydrophilic Wire Guide Recalled by Cook Inc. Due to...
The Issue: Potential coating contamination with glass particles.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Molift Air 205 Recalled by Moller Vital Due to Potential for the bolt on the...
The Issue: Potential for the bolt on the suspension coupling on the Molift Air to come...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adaptor for Small Battery Drive and Small Battery Drive II. Recalled by The...
The Issue: There was a potential for the Adaptor and Light Adaptor for Small Battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.