Product Recalls in Missouri
Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,937 recalls have been distributed to Missouri in the last 12 months.
Showing 20841–20860 of 29,298 recalls
Recalled Item: White Lumax Guiding Coaxial Catheter Catheter Recalled by Cook Inc. Due to...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kumpe Access Catheter Cathether Recalled by Cook Inc. Due to Increase in...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beacon Tip Royal Flush Plus High-Flow Catheter Catheter Recalled by Cook...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shuttle Select Slip-Cath Catheter Recalled by Cook Inc. Due to Increase in...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aprima Access Nonvascular Introducer Set Accessories Recalled by Cook Inc....
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESTREAM Image Suite V3: MINI-PACS/F IMG ST/CLASSIC: REF/Catalog # 1036490...
The Issue: Carestream Health received a complaint related to CARESTREAM Image Suite 4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESTREAM Image Suite V4 Recalled by Carestream Health Inc Due to...
The Issue: Carestream Health received a complaint related to CARESTREAM Image Suite 4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neff DAgostino Percutaneous Access Set Accessories Recalled by Cook Inc. Due...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FluoroSet Radiographic Tubal Assessment Set Cannula Recalled by Cook Inc....
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beacon Tip Torcon NB Advantage Catheter Catheter Recalled by Cook Inc. Due...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Frostie Heated Gloves (All sizes) Deep penetrating heat...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Unisex Rechargeable Heated Slipper (All sizes) Deep...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Heated Slipper Gray (All sizes) Deep penetrating heat...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Heated Slipper (All sizes) Deep penetrating heat garment...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00720504022 ACETAB.CUPW/SH Recalled by Zimmer Trabecular Metal Technology,...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POROUS PATELLA 32MM X 10MM - 00587806532 POROUS PATELLA 35MM Recalled by...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Given Imaging Bravo¿¿ pH capsule delivery device Recalled by Covidien LLC...
The Issue: Potential of an allergic reaction in a patient with nickel sensitivity.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REV. SHELL LINER 0D 28X48 00700504828 REV. SHELL LINER 10D Recalled by...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to Potential...
The Issue: Potential non-recoverable loss of image acquisition. The affected Discovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Given Imaging Bravo¿ pH capsule delivery device Recalled by Covidien LLC Due...
The Issue: Potential of an allergic reaction in a patient with nickel sensitivity.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.