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. 1,638 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
1,638 in last 12 months

Showing 4528145300 of 47,027 recalls

Medical DeviceSeptember 14, 2012· Sorin Group USA, Inc.

Recalled Item: Gish 3/8 x 3/8" Straight Connector with Luer fitting Recalled by Sorin Group...

The Issue: Due to a molding irregularity, certain lots of connectors have the potential...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX PENTRA Creatinine 120 CP Recalled by Horiba Instruments, Inc dba Horiba...

The Issue: This recall was initiated because some customers were experiencing an alarm...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceSeptember 14, 2012· Zimmer, Inc.

Recalled Item: Trilogy Acetabular AB Shells with Cluster Holes. The Trilogy Acetabular...

The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Zimmer, Inc.

Recalled Item: Trilogy Acetabular Shells with Holes. The Trilogy Acetabular System is...

The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodSeptember 14, 2012· Food Source, Inc

Recalled Item: Tomorrow's Tropicals Mangos Distributed by FoodSource A C.H. Robinson...

The Issue: Out of an abundance of caution, the firm is voluntarily recalling mangoes...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 13, 2012· McCormick & Company, Inc.

Recalled Item: Zatarain's New Orleans Style Beef Flavor Rice Mix Recalled by McCormick &...

The Issue: Food product containing wheat was packaged into containers which do not...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 13, 2012· McCormick & Company, Inc.

Recalled Item: Zatarain's Chicken/Cheddar Brocolli Mix Recalled by McCormick & Company,...

The Issue: Food product containing wheat was packaged into containers which do not...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 13, 2012· McCormick & Company, Inc.

Recalled Item: Zatarain's New Orleans Style Chicken Flavor Rice Mix Recalled by McCormick &...

The Issue: Food product containing wheat was packaged into containers which do not...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 13, 2012· OrthoPediatrics Corp

Recalled Item: Trochar Scalpel Instrument (Surgical Punch) OrthoPediatrics intramedullary...

The Issue: A complaint received from sales representative that a replenishment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2012· Zimmer, Inc.

Recalled Item: CPT Hip System Femoral Stem Petite Recalled by Zimmer, Inc. Due to Zimmer...

The Issue: Zimmer Inc. is initiating a removal of the CPT Modular Stem (item...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2012· Zimmer, Inc.

Recalled Item: CPT Modular Stem Recalled by Zimmer, Inc. Due to Zimmer Inc. is initiating a...

The Issue: Zimmer Inc. is initiating a removal of the CPT Modular Stem (item...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2012· Heartsine Technologies, Limited

Recalled Item: HeartSine Samaritan(R) 300/300P PAD devices with serial numbers 0400000501...

The Issue: Certain Samaritan 300/300P PAD devices may experience one or both of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 13, 2012· Zimmer, Inc.

Recalled Item: CPT Femoral Stem 12/14 Neck Taper Extended Offset Recalled by Zimmer, Inc....

The Issue: Zimmer Inc. is initiating a removal of the CPT Modular Stem (item...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2012· 3M Company - Health Care Business

Recalled Item: 3M Steri-Vac Gas Sterilizer/Aerator models 5XL and 8XL. 3M Steri-Vac...

The Issue: 3M determined that the electrical grounding mechanism for the Steri-Vac 5XL...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Magnetom Skyra Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: When positioning the Flex Large 4 Coil (part No. 8625761) off-center in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2012· Philips Healthcare Inc.

Recalled Item: Philips Digital Diagnost with patient carriage Model: 712050 with serial...

The Issue: Hook does not securely hold the footplate in vertical position, causing the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugSeptember 12, 2012· Sandoz Incorporated

Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by Sandoz Incorporated Due to...

The Issue: Impurities/Degradation Products: An out of specification result for a known...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 12, 2012· Sandoz Incorporated

Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by Sandoz Incorporated Due to...

The Issue: Impurities/Degradation Products: An out of specification result for a known...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 11, 2012· Philips Healthcare Inc.

Recalled Item: Philips HeartStart XL M4735A Defibrillator/Monitors Recalled by Philips...

The Issue: HeartStart XL Defibrillator/Monitor (M4735A) used on a patient when AC power...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur BR Assay: Catalog Number: US: Recalled by Siemens...

The Issue: BR Assay for CA 27.29 Calibration Interval Change due quality control (QC)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing