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. 1,747 recalls have been distributed to Missouri in the last 12 months.
Showing 47741–47760 of 52,570 recalls
Recalled Item: PHEnFX (TM) Recalled by Beta Labs Due to The products contain DMAA, also...
The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Oxyphen XR Recalled by Beta Labs Due to The products contain DMAA, also...
The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PHENTALENE (TM) Recalled by Beta Labs Due to The products contain DMAA, also...
The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RED VIPERS Recalled by Beta Labs Due to The products contain DMAA, also...
The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VERSA-FX II FEMORAL FIXATION SYSTEM COMPRESSION TUBE/PLATE Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Free Lock Femoral Hip Fixation System Compression Tube/Plate Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Healthcare...
The Issue: The MRx may deliver a non-synchronized cardioversion shock resulting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX FEMORAL FIXATION SYSTEM COMPRESSION LAG SCREW Recalled by Zimmer,...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500 and Dimension Vista 1500 System Aliquot Well Recalled by...
The Issue: Siemens is conducting a field correction for Dimension Vista 500 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX II FEMORAL FIXATION SYSTEM COMPRESSION TUBE/PLATE Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX Revolution Recalled by Carestream Health Inc. Due to Carestream Health...
The Issue: Carestream Health Inc. is conducting a recall for the Column end Cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Suction Wand Recalled by Edwards Lifesciences, LLC Due...
The Issue: Edwards is recalling certain lots of Rigid Suction Wands because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery IGS 730 Cardiovascular X-Ray Imaging System. The...
The Issue: GE Healthcare has recently become aware of a potential safety issue with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Free Lock Femoral Hip Fixation System Compression Lag Screw . Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmBisome (amphotericin B) liposome for injection Recalled by Astellas Pharma...
The Issue: Lack of Assurance of Sterility; Astellas Pharma US, Inc. is performing a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NeoCitran Extra Strength Cold & Flu (acetaminophen 650 mg Recalled by...
The Issue: Presence of Foreign Substance: The products are being recalled because they...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Theraflu Exte (dextromethorphan hydrobromide 20 mg Recalled by Novartis...
The Issue: Presence of Foreign Substance: The products are being recalled because they...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Theraflu Nighttime Severe Cold & Cough (acetaminophen 650 mg Recalled by...
The Issue: Presence of Foreign Substance: The products are being recalled because they...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Theraflu Flu & Sore Throat (acetaminophen 650 mg Recalled by Novartis...
The Issue: Presence of Foreign Substance: The products are being recalled because they...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amoxicillin for Oral Suspension Recalled by Teva Pharmaceuticals USA, Inc....
The Issue: Discoloration: This recall is being carried out due to an orange to brown...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.