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 28521–28540 of 29,186 recalls
Recalled Item: T5 Hytrel Zipper Toga. Product Usage: The togas are intended Recalled by...
The Issue: The clear tape, that is intended to aid in the prevention of patients fluids...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 8.5" (215.9mm) Serrated 1.0 mm Tips...
The Issue: Firm officials reported to CIN-DO that their Electrosurgical Monopolar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Non-Insulated Tips Recalled by PSC...
The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex XE-5000 Automated Hematology System Recalled by Sysmex America, Inc....
The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex XE-2100C Automated Hematology System Recalled by Sysmex America, Inc....
The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 7.75" (196.9 mm) 0.5 mm Tips Non-Stick...
The Issue: Firm officials reported to CIN-DO that their Bipolar Bayonet Forceps 7.75"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Insulated Tips Recalled by PSC...
The Issue: Firm officials reported to CIN-DO that the outer carton label of this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-Flow ON-Q Pain Relief System Recalled by I-Flow LLC Due to I-Flow...
The Issue: I-Flow initiated two voluntary product removals of the ON-Q Pain Relief...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Irrigating Bayonet Forceps 8.25" (209.6 mm) 1.5 mm Tips Recalled by PSC...
The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Spinal System Lamina Hooks Synthes Medium TI Lamina Hook Recalled...
The Issue: USS Lamina Hooks, Medium, Right are being recalled because the hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT CA 19-9XR Reagent Kit Recalled by Abbott Laboratories Due to The...
The Issue: The six ARCHITECT CA 19-9XR reagent lots are demonstrating a shift up in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Divided Cannula end tidal C)2 sampling w/male luer-lock connector. 7...
The Issue: A complaint was received, and later verified, that product labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Isothermal Breathing Circuit Recalled by Carefusion 2200 Inc Due to...
The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Isothermal Breathing Circuit Recalled by Carefusion 2200 Inc Due to...
The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advantage Workstation Volume Share 2 (versionAW4.4_04) with Volume Viewer 3...
The Issue: GE Healthcare has became aware of two issues with the Advantage Workstation....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Isothermal Breathing Circuit Accessory - Infant Patient Y Connector...
The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbiologics 217 Osseo Avenue North Recalled by Microbiologics Inc Due to...
The Issue: Microbiologics is recalling a number of lots of KWIK-QC Gram Stain Slides....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo(R) Lab Data Manager and syngo(R) Lab Process Manager Recalled by...
The Issue: When using the syngo Quality Control package the system may not perform as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinity Biotech Recalled by Clark Laboratories, Inc. (dba,Trinity Biotech...
The Issue: The Positive Control for the Captia Varicella-Zoster Virus (VZV) IgG Kit has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyLink Informatic System is included with the Dimension Vista System....
The Issue: When using the EasyLink Quality Control Package the system may not perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.