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. 2,530 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,530 in last 12 months

Showing 2690126920 of 29,284 recalls

Medical DeviceMay 30, 2013· Hill-Rom, Inc.

Recalled Item: TotalCare Bed used with AccuMax Quantum VPC mattress AccuMax Quantum...

The Issue: When the bed is put into the chair egress position, the magnets on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2013· Linvatec Corp. dba ConMed Linvatec

Recalled Item: ******APEX Arthroscopy Tubing Set. Intended for use for joint Recalled by...

The Issue: Conmed Linvatec received complaints that their products C7120 APEX...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2013· Linvatec Corp. dba ConMed Linvatec

Recalled Item: ******QTY 1***APEX Arthroscopy Tubing Set. Intended for use for Recalled by...

The Issue: Conmed Linvatec received complaints that their products C7120 APEX...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens MEVATRON series Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: The information regarding the FILM Mode calibration may have been considered...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· DJO, LLC

Recalled Item: VenaFlow Elite 30B-B and 30BI-B Product Usage: The VenaFlow Elite Recalled...

The Issue: DJO, LLC has recently identified a product safety issue with the battery...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Medtronic Sofamor Danek USA Inc

Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...

The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Abbott Medical Optics, Inc.

Recalled Item: STAR S3 ActiveTrack Excimer System (STAR S3) Mfg by AMO Manufacturing USA...

The Issue: Under specific conditions, there is an unlikely potential to result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Medtronic Sofamor Danek USA Inc

Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...

The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Beckman Coulter Inc.

Recalled Item: SYNCHRON System(s) Lactate (LACT) Reagent. Product Usage: Lactate (LACT)...

The Issue: Beckman Coulter has confirmed customer reports of LACT Lot M210077 failing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Medtronic Sofamor Danek USA Inc

Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...

The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Boston Scientific Corporation

Recalled Item: NephroMax high Pressure nephrostomy Balloon Catheter Kit. Material...

The Issue: Incorrect sized renal sheath was packaged with the NephroMax high pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Boston Scientific Corporation

Recalled Item: Alair Bronchial Thermoplasty Catheter Recalled by Boston Scientific...

The Issue: Boston Scientific has discovered an inconsistent "Use By" expiration date on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Boston Scientific Corporation

Recalled Item: RigiflexTM 11 Single-Use Achalasia Balloon Dilator Recalled by Boston...

The Issue: Product labeled with incorrect expiration date.

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

Class III — Low RiskOngoing
Medical DeviceMay 28, 2013· Bard Peripheral Vascular Inc

Recalled Item: BARD PERIPHERAL VASCULAR VACCESS¿ PTA Balloon Dilatation Catheters Recalled...

The Issue: Bard Peripheral Vascular (BPV) has confirmed that some product code/lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Medtronic Sofamor Danek USA Inc

Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...

The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Dental EZ Stardental Division

Recalled Item: StarDental Classique(TM) Diamond Dental Bur. Used for specific applications...

The Issue: Recall was initiated because a manufacturing issue was found that prevented...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Medtronic Sofamor Danek USA Inc

Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...

The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Abbott Medical Optics, Inc.

Recalled Item: STAR S4 with Variable Spot Scanning Excimer System (STAR S4) Recalled by...

The Issue: Under specific conditions, there is an unlikely potential to result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Abbott Medical Optics, Inc.

Recalled Item: STAR S4 IR Excimer System (STAR S4 IR) Mfg by AMO Manufacturing USA Recalled...

The Issue: Under specific conditions, there is an unlikely potential to result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Medtronic Sofamor Danek USA Inc

Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...

The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...

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

Class II — Potential Health HazardOngoing