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. 1,040 recalls have been distributed to Missouri in the last 12 months.
Showing 20541–20560 of 52,570 recalls
Recalled Item: Timolol Maleate Sterile Opthalmic Solution Recalled by Rising...
The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol Maleate USP Recalled by Rising Pharmaceuticals, Inc. Due to...
The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Optium EZ Blood Glucose Monitoring System Recalled by Abbott Diabetes Care,...
The Issue: Instructions sent in a letter or in instructions for use for disinfecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis Precise Nitinol Stent System. The Cordis PRECISE Nitinol Stent...
The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precision Xtra Blood Glucose & Ketone Monitoring System Recalled by Abbott...
The Issue: Instructions sent in a letter or in instructions for use for disinfecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Precision H Blood Glucose and Ketone Monitoring System Recalled by...
The Issue: Instructions sent in a letter or in instructions for use for disinfecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S.M.A.R.T. Nitinol Stent System and the S.M.A.R.T. Control Nitinol Stent...
The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis S.M.A.R.T. CONTROL /S.M.A.R.T. Vascular Stent System. The S.M.A.R.T....
The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HardyCHROM MRSA Recalled by Hardy Diagnostics Due to False Positive results...
The Issue: False Positive results due to the MSSA (methicillin-susceptible) strain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVKARE Ranitidine Tablets Recalled by AVKARE Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AVKARE Ranitidine Tablets Recalled by AVKARE Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ranitidine Oral Solution Recalled by Precision Dose Inc. Due to CGMP...
The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Silver Bullet Recalled by Natures Rx Due to Undeclared Active
The Issue: Marketed Without an Approved NDA/ANDA; Product contains undeclared active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eleganza 5 (AC powered adjustable bed) Recalled by Linet Spol. S.r.o. Due to...
The Issue: A component used within the side rail mechanism may malfunction, resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Cardiopulmonary GmbH / Getinge Quadrox-iD Pediatric Diffusion...
The Issue: Sterile barrier system may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: fentaNYL 400 mcg/200 mL (2 mcg/mL) ROPivacaine HCl 0.2% 400 Recalled by QuVa...
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Albuterol 2.5mg / Ipratropium 0.75mg /Budesonide 0.5mg Recalled by...
The Issue: Lack of Processing Controls
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 500 mcg/250 mL (2 mcg/mL) ROPivacaine HCl 0.2% 500 Recalled by QuVa...
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Albuterol 2.5mg / Ipratropium 0.75mg/ Triamcinolone 0.5 mg 3ML Vial Recalled...
The Issue: Lack of Processing Controls
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 200 mcg/100 mL (2 mcg/mL) ROPivacaine HCl 0.2% 200 Recalled by QuVa...
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.