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. 2,266 recalls have been distributed to Maine in the last 12 months.
Showing 47701–47720 of 48,770 recalls
Recalled Item: Siemens syngo(R) Lab Data Manager. The syngo(R) Lab Data Manager Recalled by...
The Issue: The recalling firm has discovered that when using a Sysmex(R) CA-7000 or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyLink(TM) Informatics System Recalled by Siemens Healthcare Diagnostics,...
The Issue: There is a potential for the EasyLink system to display and transmit to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Shot Epidural Trays Recalled by Integra LifeSciences Corp. d.b.a....
The Issue: Integra LifeSciences is recalling one lot of Single Shot Epidural Trays as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow International Recalled by Arrow International Inc Due to Arrow is...
The Issue: Arrow is recalling the product due to the possibility of voids in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diazepam Injection Recalled by Meridian Medical Technologies a Pfizer...
The Issue: Impurities/Degradation Products: High Out of Specification levels for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Siemens syngo.plaza radiological image processing system. Recalled by...
The Issue: Siemens became aware of an unintended behavior when using syngo.plaza. In...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Ultraview DM3 Monitor Model Number: 91330-NT The Ultraview DM3...
The Issue: Unit fails to power up, resulting in an equipment alarm
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL80 FLEX (with FLEX software) and ABL80 FLEX CO-OX (with Recalled by Sendx...
The Issue: The firm recalled because the glucose measurements from a patient sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Rigid Suction Wand Recalled by Edwards Lifesciences,...
The Issue: Edwards is recalling Suction Wand models SPC2081 and S033 because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kombiglyze XR (saxagliptin and metformin HCl extended-release) tablets...
The Issue: Labeling; Correct labeled product miscart/mispack: Some Physician sample...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kombiglyze XR (saxagliptin and metformin HCl extended-release) tablets...
The Issue: Labeling; Correct labeled product miscart/mispack: Some Physician sample...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Caziant (desogestrel and ethinyl estradiol) Tablets Recalled by Watson...
The Issue: Impurities/Degradation Products: High Out-of-specification results were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pitocin (Oxytocin Injection Recalled by JHP Pharmaceuticals, LLC Due to...
The Issue: Labeling: Label Mix-up: Pitocin storage conditions should be labeled, "Store...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Campbell's Oyster Stew Recalled by Campbell Soup Supply Co., LLC Due to The...
The Issue: The product has been prepared, packed, or held under insanitary conditions...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PathFinder NXT Pivoting Percutaneous Rod Holder This device is an Recalled...
The Issue: Complaints have been reported where, during surgery, the surgeon was unable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pathfinder NXT Fixed Percutaneous Rod Holder Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer is recalling Pathfinder NXT Fixed Percutaneous Rod Holder, because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Button Switchpens Recalled by PSC Industries Inc Due to The carton label for...
The Issue: The carton label for this device has the manufacturer symbol where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Button Switchpens Recalled by PSC Industries Inc Due to The Tyvek pouch...
The Issue: The Tyvek pouch label for this device states: 'with holster'; however, this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pathfinder NXT Fixed Percutaneous Rod Holder Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer is recalling Pathfinder NXT Fixed Percutaneous Rod Holder, because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trizivir (abacavir sulfate 300mg Recalled by GlaxoSmithKline Inc Due to...
The Issue: Adulterated Presence of Foreign Tablets: Trizivir 300/150/300 mg tables, Lot...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.