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. 2,477 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,477 in last 12 months

Showing 4182141840 of 52,647 recalls

Medical DeviceJanuary 15, 2015· Invacare Corporation

Recalled Item: FDX Electric Wheelchair. Invacare FDX Recalled by Invacare Corporation Due...

The Issue: If the slack in the wires is not routed and secured correctly, flexing of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2015· Invacare Corporation

Recalled Item: Storm Series Electric Wheelchair. Invacare FDX Recalled by Invacare...

The Issue: If the slack in the wires is not routed and secured correctly, flexing of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2015· Intuitive Surgical, Inc.

Recalled Item: da Vinci Si Surgical System Recalled by Intuitive Surgical, Inc. Due to The...

The Issue: The Wall chart has been updated because it was noted that Wall Chart (PN...

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

Class II — Potential Health HazardOngoing
FoodJanuary 14, 2015· J P Veggies Inc. DBA VeggieLand

Recalled Item: Chili-Bean Fresh Veggiburger Recalled by J P Veggies Inc. DBA VeggieLand Due...

The Issue: Franklin Farms DBA VeggiLand is recalling their Chili-Bean Veggiburgers...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 14, 2015· INO Therapeutics (dba Ikaria)

Recalled Item: Ikaria Recalled by INO Therapeutics (dba Ikaria) Due to Potential delivery...

The Issue: Potential delivery failure alarm condition. INOmax DSIR with software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 101 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: ADAPTOR Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUA 540 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK SW/EAU STERILE Recalled by Teleflex Medical Due to Foreign Object...

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: Hudson RCI¿ Humidifier Adaptor Recalled by Teleflex Medical Due to Foreign...

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK SW/EAU STERILE Recalled by Teleflex Medical Due to Foreign Object...

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing