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. 1,749 recalls have been distributed to Minnesota in the last 12 months.
Showing 44941–44960 of 52,120 recalls
Recalled Item: Mangiacotti - Lemon Verbena Hand Sanitizer Spray Recalled by Mangiacotti Due...
The Issue: Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mangiacotti - Pomegranate Hand Sanitizer Spray Recalled by Mangiacotti Due...
The Issue: Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mangiacotti - Ocean Hand Sanitizer Spray Recalled by Mangiacotti Due to...
The Issue: Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mangiacotti - Clementine Hand Sanitizer Spray Recalled by Mangiacotti Due to...
The Issue: Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mangiacotti - Ginger Lime Hand Sanitizer Spray Recalled by Mangiacotti Due...
The Issue: Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mangiacotti - Lavender Hand Sanitizer Spray Recalled by Mangiacotti Due to...
The Issue: Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KODAK DirectView DR 7500 Dual Detector System Recalled by Carestream Health,...
The Issue: Carestream Health, Inc. has recalled DR 7500 Dual Detector System utilizing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vital Signs Anesthesia Circuits The Ventilator Circuit is intended for...
The Issue: A circuit in use was occluded by a blue port cap that was inadvertently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon Medical Imaging Recalled by Mckesson Information Solutions LLC Due...
The Issue: Images may be archived to an incorrect or invalid archive location resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap proSA Adjustment Disc Size Large (L) The Miethke proSA Recalled by...
The Issue: The accuracy is out of specification for the Aesculap proSA Adjustment Disc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carisoprodol Tablets Recalled by Watson Laboratories Inc Due to Presence of...
The Issue: Presence of Foreign Substance; metal particulates were visually observed in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine HCl Injection Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter- Confimed customer complaint of particulates...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ACUSON SC2000 Ultrasound System Recalled by Siemens Medical Solutions USA,...
The Issue: The user interface assembly on the ACUSON SC2000 may become loose with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON SC2000 Power Input: 100-240VAC Recalled by Siemens Medical Solutions...
The Issue: The locking mechanism that is intended to hold the control panel in a fixed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orbit soft Infusion sets Recalled by Perrigo Diabetes Care Due to Perrigo...
The Issue: Perrigo was notified by our supplier, Ypsomed AG, that they are recalling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalys Precision Laser System (United States) - Catalys-U: Catalys...
The Issue: Potential for unexpected heating of the transformer mounting bolt located...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000/2000 XPi Systems Androstenedione (Test Code AND) Recalled by...
The Issue: Siemens Healthcare Diagnostics confirmed over-recovery of samples with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE/IMMULITE 1000 Systems Androstenedione (Test Code AND) Recalled by...
The Issue: Siemens Healthcare Diagnostics confirmed over-recovery of samples with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE Monitor B850 Recalled by GE Healthcare, LLC Due to There is a...
The Issue: There is a potential for communication loss associated with the F5-01 Frame...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compensator Slider Lambda 6x20 component (part number 473704-0000-000)...
The Issue: Carl Zeiss Microscopy, LLC has recalled the Compensator Slider Lamda 6x20...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.