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. 2,348 recalls have been distributed to Vermont in the last 12 months.
Showing 20361–20380 of 27,157 recalls
Recalled Item: ORTHO SPEC GRP CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-075...
The Issue: Knee brace could fail to maintain the locked position and a loss of balance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAILEY ORTHO CONTENDER POST-OP-KNEE BRACE Model : 75-7500-038 Post-Operative...
The Issue: Knee brace could fail to maintain the locked position and a loss of balance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CT ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-011 Post-Operative...
The Issue: Knee brace could fail to maintain the locked position and a loss of balance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digital Temple Thermometer labeled under: Bestmed Recalled by Bestmed, LLC...
The Issue: An incorrect calibration of the thermometer that causes the device to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRIELLE ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-087...
The Issue: Knee brace could fail to maintain the locked position and a loss of balance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care CKMB DilPak- an in vitro diagnostic product Recalled by...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care" MYO TestPak-in vitro diagnostic test for the Recalled by...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nebulizer Masks Opti-Mist and Opti-Mist Clear Nebulizer masks are intended...
The Issue: The Nebulizer mask malfunctions in that there is reduced or no aerosol...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care MYO DilPak Catalog Number: CMYO-D SMN:10445081 in...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care" CCRP TestPak-in vitro diagnostic product intended to...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care BHCG CalPak-in vitro diagnostic product intended to...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care BHCG TestPak-an in vitro diagnostic product intended...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care CTNI TestPak-in vitro diagnostic test for the Recalled by...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care pBNP TestPak- in vitro diagnostic test for Recalled by...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care CKMB TestPak- in vitro diagnostic test for Recalled by...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care DDMR TestPak Catalog Number: CDDMRE SMN: 10701511...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care CCRP CalPak-in vitro diagnostic product intended to...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare DuraDiagnost stationary X-ray system Recalled by Philips...
The Issue: The detector may signal that it is ready for acquisition when it actually is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Bone Awl Recalled by Aesculap, Inc. Due to The flexible shaft of...
The Issue: The flexible shaft of the instruments may break during orthopedic spinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arctic Sun 5000 and Arctic Sun 2000 Recalled by C.R. Bard, Inc. Due to...
The Issue: Improper targeted temperature therapy was delivered to patients because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.