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.
Showing 24141–24160 of 29,284 recalls
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM PERMANENT CAUTERY HOOK Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyberKnife Robotic Radiosurgery System with the first generation IRIS...
The Issue: Software upgrade to correct potential safety issue related to CyberKnife...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITI VISION SYSTEM ULTRASOUND FMS. Single-use fluid management system....
The Issue: Alcon is conducting a medical device recall due to the possible presence of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crea A and B membranes Recalled by Radiometer America Inc Due to Negative...
The Issue: Negative drift on QC during in-use lifetime of CREA membranes can be observed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Esprit V1000 Ventilator and Esprit/V200 Conversion Ventilator The Esprit...
The Issue: If the power supply fan mounting screws are installed incorrectly, the ends...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammomat Inspiration system: Product Usage: mammography exams Recalled by...
The Issue: It was determined that if the Mammomat Inspiration system is not secured to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soft Contact Lens Recalled by Cooper Vision Caribbean Corp. Due to Portions...
The Issue: Portions of the lots may contain units with an incorrect lens axis condition.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill set long Recalled by Straumann USA, LLC Due to Drill set may contain...
The Issue: Drill set may contain incorrect drill.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical LEEP RADIUS LOOP ELECTRODE (W 2.0 cm x D 1.0 cm D Recalled by...
The Issue: Outer box is mislabeled as P/N R2010- Large Radius Loop Electrode instead of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Number ASHA4730-01: Ambient HipVac 50 Wand with Integrated Finger...
The Issue: Potential breach of sterile barrier due to defective product tray.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiomat M+ NIF 14 x 17 Recalled by AGFA Healthcare Corp. Due to Some...
The Issue: Some material of the coating Type CXCPMV3 has potential artifacts showing a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Titan Reverse Shoulder System right and left head cutting templates...
The Issue: A single lot of left and a single lot of right Reverse Shoulder System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Relief ACP Oral Care Gel intended to relieve discomfort from Recalled by...
The Issue: Product sold after April 1, 2014 were inadvertently filled with hydrogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacemaker Tray (Cardiovascular Surgical Instruments convenience kit)...
The Issue: According to the recall notice received from Hospira, the recall was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Legionella Latex Test Recalled by Remel Inc Due to A reagent within...
The Issue: A reagent within the test may return false negative results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott m2000sp Recalled by Abbott Molecular Due to Some versions of...
The Issue: Some versions of Application Specifications (App Spec) are incompatible with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.