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. 1,023 recalls have been distributed to Vermont in the last 12 months.
Showing 12161–12180 of 27,157 recalls
Recalled Item: Siemens ARTIS pheno Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: The potential exists for system movement to be permanently blocked by an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow PSI Kit for use with 7 - 7.5 Fr. Catheters ASK-09801-UPM Recalled by...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ EPIDURAL CATHETERIZATION KIT AK-05000 Recalled by Arrow International...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL CATHETERIZATION COMPONENT EC-05000 Recalled by Arrow...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or...
The Issue: Monitor/Defibrillator may not deliver a shock after the "Shock" button on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow SPINAL ANESTHESIA SET ASA-25090-S Recalled by Arrow International Inc...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-17019-MSC Recalled by...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 MONITOR/DEFIBRILLATOR service kits Recalled by Physio-Control,...
The Issue: Monitor/Defibrillator may not deliver a shock after the "Shock" button on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Central Venous Catheterization Kit ASK-04200-UPM Recalled by Arrow...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL CATHETERIZATION KIT JH-05500 Recalled by Arrow International...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Lipase Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: Firm has received customer complaints regarding failed calibrations and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05500-CAN Recalled by...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Arrow¿ STIM CPNB TUOHY NDL: 18G x 14CM (5-1/2") Recalled by Arrow...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL CATHETERIZATION KIT CK-02220 Recalled by Arrow International...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL NEEDLE KIT SL-05500 Recalled by Arrow International Inc Due...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Maximal Barrier Drape ASK-00002-1A Recalled by Arrow International Inc...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow StimuCath(R) Continuous Nerve Block Kit ASK-05060-CHO1 Recalled by...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow FlexTip Plus(R) Combined Spinal Epidural Catheterization Kit...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Pressure Injectable Two-Lumen PICC Kit 5 Fr. x 50 cm EU-05052-HPMSB...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost PCF Recalled by Philips Medical Systems Gmbh, DMC Due to When...
The Issue: When using the Table Up/Down button, the system may experience Error 80,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.