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. 2,515 recalls have been distributed to Vermont in the last 12 months.
Showing 5581–5600 of 27,157 recalls
Recalled Item: Procedure pack: Presource PBDS Recalled by Cardinal Health 200, LLC Due to...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...
The Issue: A force sensor in the occlusion detector may drift out of calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...
The Issue: A force sensor in the occlusion detector may drift out of calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...
The Issue: A force sensor in the occlusion detector may drift out of calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure packs: (1) Presource Pain Tray Recalled by Cardinal Health 200,...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure packs: (1) Presource PBDS Cat. PN33BPCR2 Recalled by Cardinal...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...
The Issue: A force sensor in the occlusion detector may drift out of calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure packs: (1) Presource PBDS Recalled by Cardinal Health 200, LLC Due...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource Fistulogram Pack Recalled by Cardinal Health 200, LLC Due to Packs...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure packs: (1) Presource PBDS Recalled by Cardinal Health 200, LLC Due...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion ASSEMBLY PLUNGER CASE LEFT 1/EA Recalled by Smiths Medical ASD...
The Issue: A force sensor in the occlusion detector may drift out of calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure packs: (1) Presource PBDS Cat. PNVMNIB21 Recalled by Cardinal...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure packs: (1) Presource Portacath Pack Recalled by Cardinal Health...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion PLUNGER FLOAT PLATE Recalled by Smiths Medical ASD Inc. Due to A...
The Issue: A force sensor in the occlusion detector may drift out of calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure packs: (1) Presource PBDS Cat. PG33BTO21 Recalled by Cardinal...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: remel TODD HEWITT W. CNA (LIM BROTH) Recalled by Remel, Inc Due to On lot of...
The Issue: On lot of Todd Hewitt Broth w/CNA (LIM) may exhibit no recovery of target...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to One lot of KWIK STIK ANA (3...
The Issue: One lot of KWIK STIK ANA (3 strains) QC Set is missing one of the strains,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Guardian 2 System Product Name: Guardian System 2 Recalled by...
The Issue: A software update corrected an issue where "low" and "terminal" battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veran : Endobronchial Always on Track Models: INS-0392 AOTT 21ga Needle...
The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veran : Percutaneous Always on Track Models: INS-5040 Always-On vTrack...
The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.