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. 2,524 recalls have been distributed to Maine in the last 12 months.
Showing 8101–8120 of 27,655 recalls
Recalled Item: 11278A2 11278AK2 Flexible Ureteroscope Z20615US-BA (08-2018) Recalled by...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CYSTO-URETHRO-FIBERSCOPE CYSTOSCOPE Recalled by Karl Storz Endoscopy Due to...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11272VH-TL 11272VHK-TL HD-VIEW Flexible HD Cysto-Urethroscope Z23875US-BC...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11278VSA 11278VSAK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11274BCU1 11274BCUK1 Flexible Cystoscope Z18449US-BD (08-2018) Recalled by...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11272VUE 11272VUEK Flexible Video Cysto-Urethroscope 96136031USCA V1.1...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11001RD1 11001RDK1 KARL STORZ Slim Nasopharyngolaryngoscope 96216006US V5.0...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11272VN 11272VNK Flexible Video Urethro Cystoscope Z18442US-BD (08/2018)...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11278V 11278VK CMOS Video Ureteroscope Z17744US-A (04/2016) Recalled by Karl...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Celltrion DiaTrust COVID-19 Ag Rapid Test Recalled by CELLTRION USA INC Due...
The Issue: Point of Care (PoC) rapid test products were distributed to customers who...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical H/S ELLIPTOSPHERE CATH 5 Fr -For administering contrast...
The Issue: Incorrect bonding material used for assembly of the catheter, may fail,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical H/S ELLIPTOSPHERE CATH 5 FR Set-For administering contrast...
The Issue: Incorrect bonding material used for assembly of the catheter, may fail,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical H/S CATHETER SET FR 5 with Integated Stylet Model: Recalled...
The Issue: Incorrect bonding material used for assembly of the catheter, may fail,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus DISPOSABLE GRASPING FORCEPS Recalled by Olympus Corporation of the...
The Issue: Forceps do not comply with Olympus standards for the amount of force...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon Tritanium Tibial Component (Size 6) Recalled by Howmedica...
The Issue: Stryker has discovered a potential product mix where the size of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with...
The Issue: The Implantable Neurostimulator Model may be susceptible to not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percept PC BrainSense Implantable Neurostimulator (INS) Model B35200...
The Issue: The Implantable Neurostimulator (INS) cannot communicate with the clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare TDX SP2 Recalled by Invacare Corporation Due to The battery wiring...
The Issue: The battery wiring harness on affected wheelchairs may become disconnected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroMARK Breast Biopsy Marker Recalled by Devicor Medical Products Inc Due...
The Issue: Small patient labels do not match the primary device label. The primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percept BrainSense Implantable Neurostimulator (INS) Recalled by Medtronic...
The Issue: The Implantable Neurostimulator (INS) cannot communicate with the clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.