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. 922 recalls have been distributed to Missouri in the last 12 months.
Showing 46981–47000 of 52,570 recalls
Recalled Item: Leica Ceiling Mount MS-1F & MC-1F for use with the Recalled by Leica...
The Issue: The ceiling mount supplier encountered an event in which the drive screw in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rotoprone therapy System is an advanced patient care system Recalled by...
The Issue: The lock pin can become stuck in the "in" position during the manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harvest Graft Delivery System Recalled by Harvest Technologies Corporation...
The Issue: Potential for leur connector to leak or have cracks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P21x/5-1 MHz transducer Recalled by SonoSite, Inc. Due to FUJIFILM SonoSite...
The Issue: FUJIFILM SonoSite Inc. remove P21x/5-1 Transducer because the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Ceiling Mount MSF-1 for use with M841 and M501 Recalled by Leica...
The Issue: The ceiling mount supplier encountered an event in which the drive screw in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Risperdal CONSTA (risperiDONE) Recalled by Janssen Pharmaceuticals, Inc. Due...
The Issue: Non-Sterility: Janssen is recalling one lot of Risperdal CONSTA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Loratadine 24 HR-OTC Recalled by Physicians Total Care, Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: Affected lot numbers may contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ready to Use Thymo-Cide Recalled by Wexford Labs Inc Due to Expired active...
The Issue: Expired active ingredient was used in the manufacture of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Luer Lock Cap The device is intended for use Recalled by Baxter...
The Issue: The firm is recalling lots 10043 and 10044 due to loose particulate matter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIFY¿ Dual Species Self-Contained Biological Indicator Recalled by Steris...
The Issue: STERIS has identified that the population of the G. stearothermophilus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap GNI161 Bipolar Foot Control Product Usage: The Aesculap Bipolar...
The Issue: Complaints were received for the GN161 Bipolar Foot Control reporting that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Names: Integra¿ Camino 110-4 Intracranial Pressure (ICP) Monitoring...
The Issue: Integra LifeSciences has identified through an internal evaluation that in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hospira RECEPTAL LINERS: 1L(1000mL) Recalled by Hospira Inc. Due to Hospira...
The Issue: Hospira has become aware of customers using the incorrect size Receptal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hospira RECEPTAL CANISTERS: 1L(1000mL) Recalled by Hospira Inc. Due to...
The Issue: Hospira has become aware of customers using the incorrect size Receptal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Talenti German Chocolate Cake Gelato Recalled by Talenti Gelato Due to...
The Issue: Product contains undeclared Allergen; Almonds.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Multi For Him (Full Strength Mini and Multi Softgels) Recalled by Pharmavite...
The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Multi Complete (Full Strength Mini and Multi Softgels) Recalled by...
The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Multi for Her 50+ (Full Strength Mini and Multi softgels) Recalled by...
The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Multi for Her (Full Strength Mini and Multi Softgels) Recalled by Pharmavite...
The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: *** 1) Product labeled in part: List No. 14212-28 Recalled by Hospira Inc....
The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.