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. 2,355 recalls have been distributed to Maine in the last 12 months.
Showing 25761–25780 of 27,655 recalls
Recalled Item: STERRAD 200 Sterilization System Recalled by Advanced Sterilization Products...
The Issue: The recall was initiated because Advanced Sterilization Products (ASP) has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Pumps Model Numbers: MMT-511...
The Issue: Medtronic is recalling the Medtronic Paradigm Insulin Pump because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD 100NX Sterilization System Recalled by Advanced Sterilization...
The Issue: The recall was initiated because Advanced Sterilization Products (ASP) has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: During infusions of 2.0 mL/hr the motor assembly may rotate backwards...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 64 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: If the operator selects a patient name from the worklist using the mouse and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: During infusions of 2.0 mL/hr the motor assembly may rotate backwards...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Uni Knee System Recalled by Biomet U.K., Ltd. Due to Investigation of...
The Issue: Investigation of complaints found excessive use of the instrument could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HORIBA ABX PENTRA 400 I.S.E. Module Recalled by Horiba Instruments, Inc dba...
The Issue: HORIBA Medical is informing all ABX PENTRA 400 Analyzer with I.S.E. Module...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to Some patients are...
The Issue: Some patients are obtaining access to the dosage reset codes required to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accuray CyberKnife System Medical Physicist Recalled by Accuray Incorporated...
The Issue: A defect on the master-side connector block of the pneumatic tool changer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to Some patients are...
The Issue: Some patients are obtaining access to the dosage reset codes required to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARGENT SURGICAL SYSTEMS***BIOPSY Punches*** Disposable manual instrument for...
The Issue: Due to lack of sterilization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Ojemann Cortical Stimulator Recalled by Integra Burlington MA, Inc....
The Issue: If the headphone jack is in use during a surgical procedure with the OCS2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shimadzu Corporation - Mobile DaRt Evolution This device is a Recalled by...
The Issue: The recall was initiated because Shimadzu Corporation has identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.