Product Recalls in Massachusetts

Product recalls affecting Massachusetts — including food, drugs, consumer products, medical devices, and vehicles distributed to Massachusetts. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,542 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,542 in last 12 months

Showing 2548125500 of 52,647 recalls

FoodSeptember 27, 2018· Aldi Inc

Recalled Item: Millville Maple & Brown Sugar Instant Oatmeal 15.1 oz. 10 Recalled by Aldi...

The Issue: Complaints of insects in product

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 27, 2018· GE Healthcare, LLC

Recalled Item: Aisys Anesthesia System. Sold under the following product names: AISYS...

The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· GE Healthcare, LLC

Recalled Item: Aisys CS2 Anesthesia System. Sold under the following product names: AISYS...

The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· GE Healthcare, LLC

Recalled Item: Touchscreen display kit. Sold under the following product names: TOUCHSCREEN...

The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...

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

Class II — Potential Health HazardOngoing
DrugSeptember 26, 2018· GLAXOSMITHKLINE NEBRASKA

Recalled Item: Prevacid 24HR (Lansoprazole) delayed-release capsules Recalled by...

The Issue: CGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 26, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH 930 Analyzer. In vitro diagnostic testing of clinical Recalled...

The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1300 Analyzer. In vitro diagnostic testing of clinical Recalled...

The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1600 Analyzer: In vitro diagnostic testing of clinical Recalled...

The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica Sample Handler Prime. In vitro diagnostic testing of clinical...

The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2018· Medtronic Navigation, Inc.

Recalled Item: StealthStation Cranial and Synergy Cranial Depth Gauge: StealthStation...

The Issue: An incorrect display of the Biopsy Depth Gauge graphical representation in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 26, 2018· Becton Dickinson & Company

Recalled Item: PCEA Kit ASV Yellow Stripe Microbore Recalled by Becton Dickinson & Company...

The Issue: The products have the potential to leak between the connection of the male...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2018· Oscor, Inc.

Recalled Item: TB Series Bipolar Pacing Leads Recalled by Oscor, Inc. Due to During the use...

The Issue: During the use of some TB - Temporary Bipolar Pacing Leads, featuring the...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 26, 2018· Becton Dickinson & Company

Recalled Item: PCEA ASV Yellow Microbore Recalled by Becton Dickinson & Company Due to The...

The Issue: The products have the potential to leak between the connection of the male...

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

Class II — Potential Health HazardOngoing
DrugSeptember 25, 2018· RXQ Compounding LLC

Recalled Item: Lidocaine 1% + Epinephrine 1:100 Recalled by RXQ Compounding LLC Due to...

The Issue: Subpotent drug: During testing of the retention sample, the firm discovered...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 25, 2018· Baxter Healthcare Corporation

Recalled Item: Levofloxacin Injection in 5% Dextrose Recalled by Baxter Healthcare...

The Issue: Superpotent Drug: High out of specification results for levofloxacin...

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

Class III — Low RiskOngoing
Refund
FoodSeptember 25, 2018· Whole Foods Market

Recalled Item: 365 Everyday Value Brand White Corn Chips Recalled by Whole Foods Market Due...

The Issue: Product may contain undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 25, 2018· Pro-Dex Inc

Recalled Item: PRO-DEX Surgical Driver Battery Pack PDBP-001 Series PRO-DEX Battery Pack...

The Issue: Visual particulates within a battery Tyvek pouch. The battery is provided...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· GE Healthcare, LLC

Recalled Item: Giraffe Incubator Carestation. Neonatal incubator. Device sold under the...

The Issue: Potential electric leakage affecting the user.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· GE Healthcare, LLC

Recalled Item: Panda Freestanding Warmer. Device sold under the following product names:...

The Issue: Potential electric leakage affecting the user.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· GE Healthcare, LLC

Recalled Item: Giraffe OmniBed Carestation. Neonatal incubator. Device sold under the...

The Issue: Potential electric leakage affecting the user.

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

Class II — Potential Health HazardOngoing