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. 1,945 recalls have been distributed to Missouri in the last 12 months.
Showing 21901–21920 of 52,570 recalls
Recalled Item: MICRO-TEMP LT System Recalled by Cincinnati Sub-Zero Products LLC, a...
The Issue: Updated Manual-Warnigs have been added stating that exceeding 40'C for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methylergonovine Maleate USP 0.2 mg Tablets a) 12 count (NDC Recalled by...
The Issue: Presence of Foreign Tablet/Capsule; one Promethazine tablet was found in a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corporation...
The Issue: Lack of Assurance of Sterility: Bags have potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fennel Whole Seed was packaged in a clear plastic bag Recalled by Mountain...
The Issue: Fennel Whole Seed is recalled due to a potential for contamination with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Great Value Chopped Spinach Recalled by National Frozen Foods Corporation...
The Issue: Spinach was recalled due to a potential for contamination with Listeria...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Arrow AGB+ Multi-Lumen CVC Kit-catheter permits venous access to central...
The Issue: Arrow AGB+ Multi-Lumen CVC Kit - lidstock incorrectly states within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas e 601 module (cobas 6000 Modular Series system) Part Number:...
The Issue: Quality issue with high pressure solenoid valves may cause inaccurate results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas c513 Analyzer Recalled by Roche Diagnostics Operations, Inc. Due to...
The Issue: Quality issue with high pressure solenoid valves
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas 8000 Modular Analyzer Series: cobas 8000 ISE module part Recalled by...
The Issue: Quality issue with high pressure solenoid valves
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IGuide System Recalled by Medical Intelligence Medizintechnik Gmbh Due to...
The Issue: Sometimes, although the HexaPOD has reached the target position, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tamsulosin Hydrochloride Capsules Recalled by Macleods Pharma Usa Inc Due to...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol- Dorzolamide- Latanoprost P-F (0.5/2.0/0.005%) ophthalmic drops...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol-Latanoprost P-F (0.5/0.005%) ophthalmic drops Recalled by ImprimisRx...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin and Triamcinolone Acetonide Cream USP100 Recalled by Lupin...
The Issue: Failed Content Uniformity Specifications: Out-of-specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Autoject EI Recalled by Owen Mumford USA, Inc. Due to There is a possible...
The Issue: There is a possible assembly error on Autoject EI, lot number V14. This lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Petfine Auto Injector Recalled by Owen Mumford USA, Inc. Due to There is a...
The Issue: There is a possible assembly error on Autoject EI, lot number V14. This lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max Enteric Viral Panel RUO Recalled by Becton Dickinson & Co. Due to...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max StaphSR Recalled by Becton Dickinson & Co. Due to The foil bags...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max ExK DNA 1 USA Recalled by Becton Dickinson & Co. Due to The foil...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit EXT Enteric Bacterial Panel Recalled by Becton Dickinson & Co. Due to...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.