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. 2,715 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
2,715 in last 12 months

Showing 421440 of 52,570 recalls

Medical DeviceDecember 19, 2025· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery-Enhanced Delivery System - 8mm x 8mm Recalled...

The Issue: Increased reports of stent deployment and expansion issues. The most common...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2025· Canon Medical System, USA, INC.

Recalled Item: Alphenix INFX-8000F Recalled by Canon Medical System, USA, INC. Due to It...

The Issue: It has been discovered that there is a possibility that the fixing screws of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2025· Community Products, LLC

Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...

The Issue: Potential for fraying on the body support strap.

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

Class II — Potential Health HazardOngoing
DrugDecember 18, 2025· Imprimis NJOF, LLC

Recalled Item: Dexamethasone Moxifloxacin Recalled by Imprimis NJOF, LLC Due to Presence of...

The Issue: Presence of particulate matter - Glass like particles.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 18, 2025· Imprimis NJOF, LLC

Recalled Item: Dexamethasone Moxifloxacin Ketorolac Recalled by Imprimis NJOF, LLC Due to...

The Issue: Presence of particulate matter - Glass like particles.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 18, 2025· Imprimis NJOF, LLC

Recalled Item: Tri-Moxi+¿ (Triamcinolone 9mg/0.6mL Recalled by Imprimis NJOF, LLC Due to...

The Issue: Presence of particulate matter - Glass like particles.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 18, 2025· Community Products, LLC

Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...

The Issue: Potential for fraying on the body support strap.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2025· Vascutek, Ltd.

Recalled Item: Gelsoft Plus Recalled by Vascutek, Ltd. Due to Gelatin sealed woven...

The Issue: Gelatin sealed woven polyester prostheses devices, designed for vascular...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2025· Community Products, LLC

Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...

The Issue: Potential for fraying on the body support strap.

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

Class II — Potential Health HazardOngoing
FoodDecember 17, 2025· ZIYAD BROTHERS IMPORTING

Recalled Item: Baraka Gourmet Pastry Kunafe 6.7oz. Recalled by ZIYAD BROTHERS IMPORTING Due...

The Issue: May contain partially hydrogenated oils

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: Fixone Biocomposite Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: Fixone Hybrid Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
DrugDecember 17, 2025· CareFusion 213, LLC

Recalled Item: BD ChloraPrep" Triple Swabsticks (Chlorhexidine gluconate (CHG) Recalled by...

The Issue: Lack of Assurance of Sterlity

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 17, 2025· ZIYAD BROTHERS IMPORTING

Recalled Item: Baraka French Style Puff Pastry 1lb and 1.5lbs sizes Recalled by ZIYAD...

The Issue: May contain partially hydrogenated oils

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: AlternatiV+ Screw-In Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: Genesis Knotless Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: AlternatiV+ Max Knotless Anchor Recalled by Aju Pharm Co., Ltd. Due to...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: Genesis Dual Thread Screw-In Anchor Recalled by Aju Pharm Co., Ltd. Due to...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: Genesis Push-In Suture Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: Genesis Screw-In Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing