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. 2,137 recalls have been distributed to Missouri in the last 12 months.
Showing 2321–2340 of 52,570 recalls
Recalled Item: Philips 3D9-3v Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ketorolac Tromethamine Ophthalmic Solution Recalled by Apotex Corp. Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips L9-3 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Long Nail Recalled by Stryker GmbH Due to Investigation confirmed that the...
The Issue: Investigation confirmed that the GAMMA4 Right Long Nail was manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips S5-1 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips eL18-4 EMT Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips V6-2 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips S7-2 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI OneView System BPM Probe: Cat. No. CDI753 - CDI OneView BPM Probe...
The Issue: Due to an error in assembly of the thermistor within some units, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Casa Mamita Recalled by Camerican International Inc Due to Undeclared Allergen
The Issue: Undeclared Allergen (Milk). Consumer found a breaded halloumi Cheese Stick...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Philips C9-5EC Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips S7-3t Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluoxetine Tablets Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Tablets Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Fresenius Medical Care Holdings,...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KWIK-STICK Recalled by Microbiologics Inc Due to Affected products were...
The Issue: Affected products were packaged with the incorrect KWIK STIK assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm O2 Imaging System. Mobile X-Ray System. Recalled by Medtronic...
The Issue: A mechanical component that supports the O2 gantry to the support structure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Super Cereal Plus fortified corn soya blend Recalled by East Africa...
The Issue: Products held under insanitary conditions
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nootri Toto Recalled by East Africa Boutique, LLC. Due to Products held...
The Issue: Products held under insanitary conditions
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SIGNA PET/MR Recalled by GE Medical Systems, LLC Due to GE HealthCare has...
The Issue: GE HealthCare has become aware that gradient coils for certain MR systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.