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. 1,937 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,937 in last 12 months

Showing 2298123000 of 52,570 recalls

DrugMay 2, 2019· Unipharma, Llc.

Recalled Item: DrKids Children's Natural Cough Syrup English Ivy Leaf Organic Agave...

The Issue: CGMP Deviations: Recall as a precautionary measure due to potential risk of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodMay 2, 2019· Dole Fresh Vegetables

Recalled Item: Dole Colourful Coleslaw ( Salade Chou Coloree) - Canada Shredded Recalled by...

The Issue: Complaints received of irregular pieces of soft plastic in the product.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMay 2, 2019· Dole Fresh Vegetables

Recalled Item: Dole Classic Coleslaw (US) Shredded cabbage and carrots. 14 oz. US Recalled...

The Issue: Complaints received of irregular pieces of soft plastic in the product.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 2, 2019· Becton Dickinson & Company

Recalled Item: CareFusion MaxPlus Clear Needleless Connector. Intended for Positive...

The Issue: After disconnection of a luer, the valve of the connector remains recessed;...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· SenTec AG

Recalled Item: SenTec Standard Starter Set with and without Service Gas (2 Recalled by...

The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· SenTec AG

Recalled Item: SenTec Membrane Changer (reloadable) [9 pcs] - Product Usage: Is Recalled by...

The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· SenTec AG

Recalled Item: SenTec Neonatal Starter Set with and without Service Gas (2 Recalled by...

The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· SenTec AG

Recalled Item: SenTec Membrane Changer Set (1 charger plus 1 insert) - Recalled by SenTec...

The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· SenTec AG

Recalled Item: SenTec Membrane Changer Insert [5 pcs - Product Usage: is Recalled by SenTec...

The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Rinovum Women's Health

Recalled Item: Revive Reusable Bladder Support Recalled by Rinovum Women's Health Due to...

The Issue: The product is unable to meet the use life of 31 cycles and may split or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Oakworks Inc

Recalled Item: OAKWORKS Inc.Lithotripsy/Urology Table: CFLU401 Recalled by Oakworks Inc Due...

The Issue: Table assembly error with incorrect actuators for the lateral and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodMay 1, 2019· U.S. Tov, Inc.

Recalled Item: Dragonfly Dehydrate Guava Ing: Guava Recalled by U.S. Tov, Inc. Due to...

The Issue: Undeclared sulfites.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceMay 1, 2019· Abbott Laboratories, Inc

Recalled Item: ARCHITECT C System Mixer - Product Usage: The ARCHITECT Clinical Recalled by...

The Issue: Mixer blade may separate from mixer due to the screw and nut failure and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2019· Medtronic Navigation, Inc.-Littleton

Recalled Item: Medtronic 0-arm TM 1000 Imaging Systems: Bl-700-00027-XXX and...

The Issue: The 0-arm 1000 Imaging System uses energy from the batteries to generate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing