Product Recalls in Maine

Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,317 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,317 in last 12 months

Showing 4044140460 of 48,770 recalls

Medical DeviceJuly 2, 2014· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....

The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 2, 2014· Mentor Texas, LP.

Recalled Item: EN MENTOR Round High Profile Single Use Saline Breast Implant Recalled by...

The Issue: The device labeling is stamped with 330cc and the device is actually 380cc...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2014· Smith & Nephew, Inc.

Recalled Item: TRIGEN(R) INTERTAN(TM) 10MM X 18 CM NAIL Recalled by Smith & Nephew, Inc....

The Issue: There was an error in manufacturing which resulted in the proximal lag screw...

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

Class II — Potential Health HazardOngoing
DrugJuly 1, 2014· American Health Packaging

Recalled Item: Ibuprofen Tablets Recalled by American Health Packaging Due to Labeling:...

The Issue: Labeling: Label Mix-Up: Some cartons of AHP Ibuprofen Tablets, USP, 600mg,...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 1, 2014· American Health Packaging

Recalled Item: Oxcarbazepine Tablets Recalled by American Health Packaging Due to Labeling:...

The Issue: Labeling: Label Mix-Up: Some cartons of AHP Ibuprofen Tablets, USP, 600mg,...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 1, 2014· PUREFRUIT CHILE S.A

Recalled Item: HyVee applesauce Recalled by PUREFRUIT CHILE S.A Due to Purefruit Chile S.A....

The Issue: Purefruit Chile S.A. is recalling pouched applesauce due to the possibility...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2014· PUREFRUIT CHILE S.A

Recalled Item: fruty U applesauce Recalled by PUREFRUIT CHILE S.A Due to Purefruit Chile...

The Issue: Purefruit Chile S.A. is recalling pouched applesauce due to the possibility...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2014· PUREFRUIT CHILE S.A

Recalled Item: Market Pantry Apple Recalled by PUREFRUIT CHILE S.A Due to Purefruit Chile...

The Issue: Purefruit Chile S.A. is recalling pouched applesauce due to the possibility...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2014· PUREFRUIT CHILE S.A

Recalled Item: fruty U applesauce Recalled by PUREFRUIT CHILE S.A Due to Purefruit Chile...

The Issue: Purefruit Chile S.A. is recalling pouched applesauce due to the possibility...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2014· PUREFRUIT CHILE S.A

Recalled Item: Market Pantry Apple Cinnamon Recalled by PUREFRUIT CHILE S.A Due to...

The Issue: Purefruit Chile S.A. is recalling pouched applesauce due to the possibility...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 1, 2014· Ansar Group, Inc. Dba Ansar Medical Technologies, Inc

Recalled Item: Blood pressure (BP) circuit of the ANSAR ANX-3.0 Autonomic Monitor Recalled...

The Issue: The blood pressure (BP) circuit occasionally fails to inflate the blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2014· Zimmer, Inc.

Recalled Item: Moore Hip Prosthesis Long Fenestrated Stem 38 mm (1-1/2 Inch) Recalled by...

The Issue: Zimmer is initiating a voluntary recall of 20 production lots of Moore Hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2014· PerkinElmer Health Sciences, Inc.

Recalled Item: Panthera-Puncher 9 . Panthera-Puncher 9 is a sample transfer instrument...

The Issue: Risk of incorrect results from samples prepared with Panthera-Puncher 9

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2014· Teleflex Medical

Recalled Item: RUSCH Recalled by Teleflex Medical Due to There is a possibility the handle...

The Issue: There is a possibility the handle of the laryngoscope may heat up and melt...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2014· Invivo Corporation

Recalled Item: Philips IP5 Information Portal The Expression Information Portal (Model IP5)...

The Issue: The wireless function of the IP5 radio could be interrupted causing loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2014· Ra Medical Systems Inc

Recalled Item: PHAROS Excimer Laser Recalled by Ra Medical Systems Inc Due to RA Medical...

The Issue: RA Medical Systems is recalling the PHAROS EX-308 Excimer Laser because...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens syngo Imaging XS Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Siemens has become aware of the potential malfunction when using syngo...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2014· Steris Corporation

Recalled Item: Reliance 1227 Cart and Utensil Washer/Disinfector Product Usage: Usage: The...

The Issue: STERIS has identified that deformation of the washers door handle pin may...

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

Class III — Low RiskOngoing
DrugJune 27, 2014· Hospira Inc.

Recalled Item: Fentanyl Citrate Injection Recalled by Hospira Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Fliptop vial crimps are loose or missing.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 27, 2014· Life Force of Tampa, LLC

Recalled Item: Life Force Chamber Product Usage:The product is intended for restful...

The Issue: The Life Force chamber is marketed and promoted as a medical device,...

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

Class II — Potential Health HazardOngoing