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. 2,489 recalls have been distributed to Minnesota in the last 12 months.
Showing 24061–24080 of 29,186 recalls
Recalled Item: Total Temporomandibular Joint Replacement System- 50mm Rt Stand Off Ti...
The Issue: Laser etching on the parts is wider and deeper than the conditions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Temporomandibular Joint Replacement System- 45mm Lft Narrow Ti Mand...
The Issue: Laser etching on the parts is wider and deeper than the conditions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Temporomandibular Joint Replacement System- 55mm Lft Standard Ti Mand...
The Issue: Laser etching on the parts is wider and deeper than the conditions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Temporomandibular Joint Replacement System- 50mm Lft Standard Ti Mandi...
The Issue: Laser etching on the parts is wider and deeper than the conditions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rapid Neg BP Combo Panel Type 3 Recalled by Siemens Healthcare Diagnostics,...
The Issue: An increase in false positive susceptible results on Rapid Neg BP Combo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Temporomandibular Joint Replacement System- 45mm Lft Standard Ti Mand...
The Issue: Laser etching on the parts is wider and deeper than the conditions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiohelp-I System Product Usage: A blood oxygenation and carbon dioxide...
The Issue: Cardiohelp- i System may have a software issue that can potentially result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroVue Bb Plus EIA is packaged as a kit which Recalled by Diagnostic...
The Issue: Samples are quantitating incorrectly, with approximately 50% higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) WWB100. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Align Radial Stems Recalled by Skeletal Dynamics Due to Report received...
The Issue: Report received where the Align Radial Stem fractured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) WW B30. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) US B100. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Patient Specific Instrument PERSONA CR Pin Guides (Femur and Recalled...
The Issue: The box of guides for a specific case arrived intact but contained two (2)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE Intuition Distal Femoral Jig Recalled by DePuy Orthopaedics, Inc. Due...
The Issue: Issuing a device correction because if the pin bushing is over loaded or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS Monarc + Subfascial Hammock with Tensioning Suture Recalled by American...
The Issue: During routine periodic packaging testing, AMS identified that in simulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AdVance"Male Sling System Recalled by American Medical Systems, Inc. Due to...
The Issue: During routine periodic packaging testing, AMS identified that in simulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlignRT- Intended for prescription use. The system is indicated for Recalled...
The Issue: Potential failure of AlignRT to assert interlock.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Infinia (including Infinia Recalled by GE Healthcare, LLC Due...
The Issue: GE is issuing this recall due to a potential safety issue related to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.