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. 2,295 recalls have been distributed to Vermont in the last 12 months.
Showing 36981–37000 of 47,027 recalls
Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...
The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT (Uninterruptible Power Supply (UPS) accessory devices)...
The Issue: The firm was notified that the failure of the UPS accessory devices used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI TF Big Bore (Uninterruptible Power Supply (UPS) accessory devices)...
The Issue: The firm was notified that the failure of the UPS accessory devices used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...
The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI TF PET/CT 16 Slice (Uninterruptible Power Supply (UPS) accessory...
The Issue: The firm was notified that the failure of the UPS accessory devices used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNESIUM SULFATE IN 5% DEXTROSE INJECTION Recalled by Hospira Inc. Due to...
The Issue: Labeling: Wrong Bar Code: There is a potential for some units to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ALL MAXAM PRODUCTS: The Maxam product is used orally in Recalled by James G....
The Issue: All Maxam brand products are recalled because it was ordered by the United...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Shanghai Ceramic Spoons Recalled by Cost Plus Management Services, Inc. Due...
The Issue: Some ceramic spoons may exceed FDA guidance levels for leachable lead and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ALL ASN products: The ASN products are in capsule or Recalled by James G....
The Issue: All ASN brand products are recalled because it was ordered by the United...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HLS/HIT Set Advanced with Bioline and/or Softline Coating Console Product...
The Issue: A potential issue was detected that could result in blood leakage from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Millennium VG Recalled by GE Healthcare Due to GE Healthcare...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpineFrontier MISquito Percutaneous Pedicle Screw System Surgical Technique...
The Issue: The PedFuse Pedicle Screw Rod Caliper included with the MISquito Pedicle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN 3000 Series Set- Huber needles. Used in combination Recalled by...
The Issue: Needle is leaking from hub/needle cannula connection
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quadrox-iD Adult Diffusion Membrane Oxygenator Product Usage: The Quadrox-iD...
The Issue: A potential issue was detected that could result in blood leakage from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge LIS software. Recalled by Merge Healthcare, Inc. Due to There is a...
The Issue: There is a potential for duplicate container numbers to be created for patients.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Confirmed finding of human hair floating in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% DEXTROSE Injection Recalled by Hospira Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: there is a potential for solution to leak at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LP Rotate Foot System prosthetic device for fitting lower extremity Recalled...
The Issue: The threads of the outer tube of the shock module of LP Rotate are too...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...
The Issue: An issue with photon dose calculation for DMLC (Dynamic MLC) plans for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LCS COMPLETE RPS inserts Recalled by DePuy Orthopaedics, Inc. Due to The LCS...
The Issue: The LCS COMPLETE RPS Knee System has higher rates of revision in Australia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.