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. 1,757 recalls have been distributed to Missouri in the last 12 months.
Showing 43361–43380 of 52,570 recalls
Recalled Item: WaterLase iPlus Dental Laser System Recalled by Biolase Technology Inc Due...
The Issue: Biolase is recalling the WaterLase iPlus Dental Laser System because of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer EDI PERIARTICULAR PLATING SYSTEM CANCELLOUS BONE SCREW Recalled by...
The Issue: Two lots of screws were commingled. Screws with etching and machining for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Extended-Release Tablets Recalled by Caraco...
The Issue: Failed Dissolution Specifications: Stability results found the product did...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Captomer-250 [succinic acid (from 250 mg DMSA)] capsules Recalled by Thorne...
The Issue: Marketed Without An Approved NDA/ANDA: Captomer and Captomer-250 are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Captomer [succinic acid (from 100 mg DMSA)] capsules Recalled by Thorne...
The Issue: Marketed Without An Approved NDA/ANDA: Captomer and Captomer-250 are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Integra¿ LED Battery Charger Recalled by Integra LifeSciences Corp. Due to...
The Issue: LED battery chargers may prematurely fail and will not charge the LED...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DATEX-OHMEDA S/5 SINGLE-WIDTH AIRWAY MODULE Recalled by GE Healthcare, LLC...
The Issue: Failure of the CO2 detector in Single-width Airway and Extension modules,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tritium Sternal Plate System Recalled by PIONEER SURGICAL TECHNOLOGY, INC....
The Issue: Lack of Sterility Assurance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prosound F75 or F75 The Hitachi Aloka Medical Recalled by Hitachi Aloka...
The Issue: Loosened monitor arm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mountain House Freeze-Dried Precooked Scrambled Eggs with Ham and Red...
The Issue: Oregon Freeze Dry, Inc. is voluntarily recalling Mountain House Scrambled...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tenor is a mobile passive lift Recalled by ARJOHUNTLEIGH POLSKA SP. ZO.O....
The Issue: ArjoHuntleigh received reports where the Tenor Lift without Scale (spreader...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTAMIX 1200 Compounder Recalled by Baxter Healthcare Corp. Due to If the...
The Issue: If the universal ingredient (UI) in an active configuration is changed using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MC-500 Multicolor Laser Photocoagulator Recalled by Nidek Inc Due to Laser...
The Issue: Laser aperture label was not affixed to device prior to shipment in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coat-A-Count Direct Androstenedione Recalled by Siemens Healthcare...
The Issue: The assay is demonstrating a higher frequency of results greater than 10...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Attest Auto-reader. Model numbers 390 Recalled by 3M Company - Health...
The Issue: Labeling on units shipped prior to May 16th, 2014 did not contain the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIS Rod 2 Recalled by Integra LifeSciences Corp. Due to Integra Lifesciences...
The Issue: Integra Lifesciences is recalling NewPort System MIS Rod, 2 because it may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Professional Bak-klene All Purpose No-Stick Bakery Spray Recalled by Plaze...
The Issue: The product contains undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CDC Anaerobe 5% Sheep Blood Agar CDC Anaerobe 5% Sheep Recalled by Becton...
The Issue: A low level of surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGFA Digital Radiography X-Ray system DX-D 100 Agfa's DX-D 100 Recalled by...
The Issue: When liquid comes in contact with the DX-D 100 touch screen, the device may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACS Canto and associated Fluidics Cart Product Usage: Flow Recalled by...
The Issue: Laser cooling fans and internal fan of the associated fluidics cart are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.