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. 2,673 recalls have been distributed to Minnesota in the last 12 months.
Showing 4501–4520 of 29,186 recalls
Recalled Item: Route 92 Medical Recalled by ROUTE 92 MEDICAL INC Due to Their is the...
The Issue: Their is the potential for distal tip separation at the proximal marker band...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Route 92 Medical Recalled by ROUTE 92 MEDICAL INC Due to Their is the...
The Issue: Their is the potential for distal tip separation at the proximal marker band...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Route 92 Medical 070 Reperfusion System Recalled by ROUTE 92 MEDICAL INC Due...
The Issue: Their is the potential for distal tip separation at the proximal marker band...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Route 92 Medical Full Length 070 Access System Recalled by ROUTE 92 MEDICAL...
The Issue: Their is the potential for distal tip separation at the proximal marker band...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Route 92 Medical Recalled by ROUTE 92 MEDICAL INC Due to Their is the...
The Issue: Their is the potential for distal tip separation at the proximal marker band...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INNOMED CUP REMOVAL STARTER INSTRUMENT Recalled by Innomed, Inc. Due to 54...
The Issue: 54 MM finisher blade was inadvertently affixed to the shaft of the CupX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...
The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...
The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...
The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...
The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe REVERSE SHOULDER Recalled by Exactech, Inc. Due to The...
The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...
The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...
The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STIK Rhizopus stolonifer (+) derived from ATCC 6227b Recalled by...
The Issue: The positive control material (Rhizopus stolonifer) within the KWIK-STIK...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe REVERSE SHOULDER Recalled by Exactech, Inc. Due to The...
The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe REVERSE SHOULDER Recalled by Exactech, Inc. Due to The...
The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...
The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe REVERSE SHOULDER Recalled by Exactech, Inc. Due to The...
The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tablo Hemodialysis System Recalled by Outset Medical, Inc. Due to...
The Issue: Hemodialysis System, pre and post dialyzer peroxide-cured silicone tubing,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...
The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.