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. 1,821 recalls have been distributed to Missouri in the last 12 months.
Showing 41481–41500 of 52,570 recalls
Recalled Item: CD8 (Leu-2a) PE (In vitro diagnostic) Recalled by BD Biosciences, Systems &...
The Issue: One lot of CD8 PE is contaminated with CD4 FITC and may cause an unexpected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The MAYFIELD¿ Ultra 360 Base Unit for head positioner Recalled by Integra...
The Issue: Through an investigation of complaints, Integra found that there is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zippie Zone Pediatric Rigid Wheelchair Model EIRZ1. Recalled by Sunrise...
The Issue: There is the potential for the height adjustable handle to dislodge due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINAC Accelerators: ARTISTE Recalled by Siemens Medical Solutions USA, Inc...
The Issue: A hardware update to replace the old PCB Assembly, Head Driver-G41 with PCB...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Starburst MRI Semi-Flex Electrode Device Recalled by Angiodynamics Due to...
The Issue: Printed mark on the trocar intended to indicate a 5cm distance from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anti-Lambda APC-H7 Recalled by BD Biosciences, Systems & Reagents Due to Two...
The Issue: Two lots of the Anti-Lambda APC-H7 antibody are contaminated with CD38 antibody.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEPFLUSH-10 (HEPARIN LOCK FLUSH SOLUTION Recalled by Fresenius Kabi USA, LLC...
The Issue: The lot failed pH specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Focal Sim radiation therapy treatment planning system Recalled by Elekta,...
The Issue: Incorrect CT to ED when using the Monaco Image Statistics Tool.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco radiation therapy treatment planning system. The Monaco system is...
The Issue: Incorrect CT to ED when using the Monaco Image Statistics Tool.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Electric Pen Drive (EPD) System Recalled by Synthes, Inc. Due to In...
The Issue: In May 2013, the original recall was initiated due to complaints the Hand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Automatic Mobile X-Ray (AMX) Series: Optima XR200 amx Recalled...
The Issue: An issue was identified with the mAs accuracy check performed on the system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Automatic Mobile X-Ray (AMX) Series: Optima XR220 amx Recalled...
The Issue: An issue was identified with the mAs accuracy check performed on the system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Automatic Mobile X-Ray (AMX) Series: Brivo XR285amx Recalled...
The Issue: An issue was identified with the mAs accuracy check performed on the system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue Information Center iX (release A.00 Recalled by Philips...
The Issue: Sp02 and/or Non Invasive Blood Pressure (NBP) alarms may become disabled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SLIM-K Recalled by Bethel Nutritional Consulting, Inc Due to Marketed...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: B-Lipo Recalled by Bethel Nutritional Consulting, Inc Due to Marketed...
The Issue: Marketed without an Approved NDA/ANDA; found to contain Lorcaserin, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 3M ESPE Clinpro 5000 (1.1% Sodium Flouride) Recalled by 3M Company/3m Espe...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date - The subject lot is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Perfect Bar Peanut Butter Recalled by Perfect Foods Bar Due to Potential...
The Issue: Perfect Bar is recalling Peanut Butter and Cranberry Crunch nutritional bars...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Perfect Bar Variety Pack (Costco Only) Recalled by Perfect Foods Bar Due to...
The Issue: Perfect Bar is recalling Peanut Butter and Cranberry Crunch nutritional bars...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dried Bean Curd Garlic Flavor 24x150g Recalled by Gemini Food Corporation...
The Issue: Gemini Foods is recalling bean curd products because they may be...
Recommended Action: Do not consume. Return to store for a refund or discard.