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. 2,505 recalls have been distributed to Minnesota in the last 12 months.
Showing 21481–21500 of 29,186 recalls
Recalled Item: Philips IntelliVue Module Measurement X2 Model: M3002A Recalled by Philips...
The Issue: The ST elevation alarm on the Patient Monitor or standalone X2 Measurement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM The product includes...
The Issue: Incorrect cannula of the sheath introducer (smaller than intended).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This reagent is for in vitro diagnostic use. Pax-5 (1EW) Recalled by Leica...
The Issue: The Bond" Polymer Detection and Novolink" Polymer Detection System may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PharmaCaribe PulmoSal 7% Sodium chloride Recalled by Pharmacaribe llc Due to...
The Issue: Vials were labeled as USP 7% Hypertonic saline instead of PulmoSal 7% (pH+)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQURE System Recalled by Radiometer America Inc Due to The AQURE System has...
The Issue: The AQURE System has a design error regarding sample type in which sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur PSA Assay Recalled by Siemens Healthcare Diagnostics, Inc Due...
The Issue: PSA assay is not meeting the High Dose Hook Effect expectation in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EliA SmDP Well Recalled by Phadia Ab Due to All equivocal and positive...
The Issue: All equivocal and positive results (greater or equal 7 EliA U/ml) on EliA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548460 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscope ED-250XL5 Operations Manual: Cleaning Recalled by Fujifilm Medical...
The Issue: This correction is in response to publicized reports of multi-drug resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscope ED-450XL5 Operation Manual: Cleaning Recalled by Fujifilm Medical...
The Issue: This correction is in response to publicized reports of multi-drug resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscope ED-250XT5 Operations Manual: Cleaning Disinfection and Storage...
The Issue: This correction is in response to publicized reports of multi-drug resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscope Recalled by Fujifilm Medical Systems U.S.A., Inc. Due to This...
The Issue: This correction is in response to publicized reports of multi-drug resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscope ED-450XT5 Operation Manual: Cleaning Recalled by Fujifilm Medical...
The Issue: This correction is in response to publicized reports of multi-drug resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Recalled by Cardinal Scale Mfg Co Due to One complaint of a seat on...
The Issue: One complaint of a seat on a scale failing unexpectedly which can cause an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Moog Curlin Infusion Recalled by MOOG Medical Devices Group Due to Moog is...
The Issue: Moog is recalling Curlin 4000, 6000, and PainSmart Infusion Pumps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548920 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548750 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548560 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549390 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548850 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.