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. 2,478 recalls have been distributed to Minnesota in the last 12 months.
Showing 27001–27020 of 29,186 recalls
Recalled Item: CONFIDENCE SPINAL CEMENT SYSTEM 5CC KIT Recalled by DePuy Spine, Inc. Due to...
The Issue: During injection of cement, the water in the hydraulic pump leaks past the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS D-Dimer Exclusion II Recalled by BioMerieux SA Due to Customer...
The Issue: Customer complaints about not repeatable results below the detection limit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) The FEMTO LDV Z2 Femtosecond Surgical Laser is an Recalled by Ziemer Usa...
The Issue: A defect in the controller board can lead to the condenser to the video...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere" hCG Combo Cassette (20/10 mIU/mL) Kit. Product Usage: The Recalled by...
The Issue: The firm initiated recall of Alere" hCG Combo Cassette (20/10 mIU/mL) kit PN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD Biopsy Systems UltraClip Dual Trigger breast tissue marker. Intended...
The Issue: Bard Peripheral Vascular (BPV) has confirmed that some devices with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DC power cable (p/n 3010556) supplied with the MEDRAD(R) Veris Recalled by...
The Issue: The firm is recalling these power cables due to a latent design reliability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom 1000 Bed Recalled by Hill-Rom, Inc. Due to Complaints have been...
The Issue: Complaints have been reported for brakes disengaging when the bed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle InsuLinx Blood Glucose Monitoring System: For In Vitro Diagnostic...
The Issue: AT rare, extremely high glucose levels (1024 mg/dL and above), the FreeStyle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray systems Product Usage: The Brilliance CT 64...
The Issue: Philips Healthcare received reports from the field that certain Brilliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liquichek" ToRCH Plus IgM Control - Positive Liquichek ToRCH Plus Recalled...
The Issue: The Liquichek" ToRCH Plus IgM Control - Positive, contains detectable levels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Hand Switch - Electric Pen Drive Recalled by Synthes USA HQ, Inc....
The Issue: Synthes received a complaint from a customer in which the Hand Switch for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL DrySlide PYR Kit Recalled by Becton Dickinson & Co. Due to In-vitro...
The Issue: In-vitro diagnostic agents were placed into incorrect packaging for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity Staple Remover Kit Recalled by Covidien LLC Due to On March 26, 2013...
The Issue: On March 26, 2013 Covidien received a recall notice from one of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL DrySlide Oxidase Kit Recalled by Becton Dickinson & Co. Due to In-vitro...
The Issue: In-vitro diagnostic agents were placed into incorrect packaging for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity I.V. Start Kit Recalled by Covidien LLC Due to On March 26, 2013...
The Issue: On March 26, 2013 Covidien received a recall notice from one of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Push...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.