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. 2,450 recalls have been distributed to Maine in the last 12 months.
Showing 18461–18480 of 48,770 recalls
Recalled Item: OSTEOVATION RMX Injectable BVF 5CC . REF/UDI: 390-6001/ /00813845021082 -...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATIONEX 5CC INJECT FORMULA. REF/UDI: 390-0005/00813845020023 - Product...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION 10CC INJECT FORMULA. REF/UDI: 390-2010/00813845020061 - Product...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION 5CC INJECT FORMULA. REF/UDI: 390-2005/00813845020054 - Product...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION 10 CC IMPACT FORMULA. REF/UDI: 390-2110/ /00813845021092 -...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION RMX 10 CC Injectable. REF/UDI: 390-6002/ /00813845021099 -...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATIONEX 2CC INJECT FORMULA. REF/UDI: 390-0002/00813845020009 - Product...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION 3CC IMPACTFORMULA. REF/UDI: 390-2103/00813845020078 - Product...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATIONEX 5CC IMPACTFORMULA. REF/UDI: 390-0205/00813845020047 - Product...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATIONEX 3CC IMPACTFORMULA. REF/UDI: 390-0203/00813845020030 - Product...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accelerator APS Aliquoter Module Recalled by Abbott Laboratories Due to In...
The Issue: In the case of an AQM clot detection error a portion of the distilled water...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe Shuttle. Upgrade Kits with part number 2109672-001 and 2109673-001...
The Issue: During Giraffe Shuttle charging, the batteries emit low concentrations of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lisinopril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: Presence of Foreign Tablet/ Capsule: Product complaint received indicating...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PRESTIGE RETRACTION GRASPER Recalled by Aesculap Implant Systems LLC Due to...
The Issue: Endoscopic graspers may become separated at the weld from handle to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION Recalled by Aesculap Implant...
The Issue: Endoscopic graspers may become separated at the weld from handle to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CKMB Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The Spanish and Swedish language versions of the IFU state that the assay...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CKMB Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The Spanish and Swedish language versions of the IFU state that the assay...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 20 mg over 9 hours...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 30 mg over 9 hours...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.