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. 2,518 recalls have been distributed to Minnesota in the last 12 months.
Showing 21161–21180 of 29,186 recalls
Recalled Item: HipLOC CHS Plate/Lag Screw Introducer Recalled by Biomet, Inc. Due to A...
The Issue: A complaint was received where the Hiploc Plate/Lag Screw Introducer was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.0 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIOS ALPHA (Image-intensified fluoroscope x-ray system) Product Usage: The...
The Issue: Siemens found a defective part in their production line which could increase...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Interlocking Bolt Recalled by Synthes (USA) Products LLC Due to...
The Issue: DePuy Synthes is initiating a voluntary medical device recall of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.5 mm and 4.0 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC Unit Recalled by CareFusion 303, Inc. Due to CareFusion is...
The Issue: CareFusion is recalling the Alaris PC unit because a component on the PC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helioseal Clear 1 x 1.25 g Recalled by Ivoclar Vivadent, Inc. Due to...
The Issue: Complaints were received claiming the material failed to polymerize under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instinct¿ Java¿ System (IFU : 046WAN0000T) . Stabilizes one or Recalled by...
The Issue: Zimmer Biomet is initiating a Medical Device Correction Notice to provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD SurePathTM Preservative Collection Vials Recalled by Becton Dickinson &...
The Issue: BD has confirmed that a portion of BD SurePath" collection vials associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammomat Inspiration with Tomosynthesis functionality Recalled by Siemens...
The Issue: A potential system fatal error may occur during tomosynthesis reconstruction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Clamp¿ System (IFU : SNA027-N-90001). Provides the stability...
The Issue: Zimmer Biomet is initiating a Medical Device Correction Notice to provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.