Product Recalls in Minnesota
Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,654 recalls have been distributed to Minnesota in the last 12 months.
Showing 8641–8660 of 29,186 recalls
Recalled Item: ATRAUMATIC ADULT LUMBAR PUNCTURE TRAY Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMBAR PUNCTURE TRAY ADULT 20G X 3.5 DP Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMBAR PUNCTURE TRAY ADULT 22G X3.5 STRL Recalled by Bard Peripheral...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray Recalled by Bard...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCA 4000 Curing Units Recalled by Envisiontec US Llc Due to The PCA 4000 may...
The Issue: The PCA 4000 may not fully cure EnvisionTEC dental resins to desired product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SyncVision Systems Recalled by Volcano Corporation Due to If FFR...
The Issue: If FFR measurement(s) are made prior to an iFR/FFR co-registration/pullback...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostic Ultrasound System Recalled by Siemens Medical Solutions USA, Inc....
The Issue: The clip store function in the ultrasound imaging system does not work when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINQ II Insertable Cardiac Monitor Recalled by Medtronic Inc., Cardiac...
The Issue: Devices may lose functionality due to susceptibility to moisture ingress.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Del(5q) Deletion FISH Probe Kit: In-Vitro Diagnostic to detect deletions...
The Issue: individual components have been labelled with incorrect colours. The red and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Collagen Plugs Recalled by Lacrimedics Inc Due to The sterile pouch seal may...
The Issue: The sterile pouch seal may contain channels that could affect the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPAQUE Herrick Lacrimal Plugs Recalled by Lacrimedics Inc Due to The sterile...
The Issue: The sterile pouch seal may contain channels that could affect the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biolox delta Ceramic V40 Femoral Head 32/ +4.0mm Catalog Number: 6570-0-232...
The Issue: Potential product mix where the size and/or offset of the Biolox delta...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biolox delta Ceramic V40 Femoral Head 32/ -4.0mm Catalog Number: 6570-0-032...
The Issue: Potential product mix where the size and/or offset of the Biolox delta...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1)Traverse Rail Carrier E-System Recalled by Hill-Rom, Inc. Due to Traverse...
The Issue: Traverse rail carriage delivered with non-conforming screws are too short to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1688 Camera Control Unit (CCU) Recalled by Stryker Corporation Due to A...
The Issue: A software defect in the camera control unit (CCU) will cause the image on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIRRUS HD-OCT Recalled by Carl Zeiss Meditec, Inc. Due to Optic nerve head...
The Issue: Optic nerve head angiography scan to be turned off due to its distribution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMASHIELD GOLD KNITTED MICROVEL DOUBLE VELOUR VASCULAR GRAFT- D: 7 mm...
The Issue: Outer labelling (HEMASHIELD GOLD Knitted Microvel Double Velour Bifurcated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BUTLER Clear Dip Recalled by Sunstar Americas, Inc. Due to Product lacks...
The Issue: Product lacks premarket clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Everest MI XT Inner Dilator Recalled by K2M, Inc Due to Stryker received two...
The Issue: Stryker received two (2) complaints for units from specific lots of Inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luscient Diagnostics 2nd Generation of COVID-19 Viral Antigen Test For...
The Issue: COVID-19 test kits (Antibody Rapid Test kit and Antigen Rapid Test Kit) are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.