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. 947 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
947 in last 12 months

Showing 40361–40380 of 52,570 recalls

Medical DeviceMarch 26, 2015· Diamedix Corporation

Recalled Item: Diamedix Is-CMV IgG Test Kit Recalled by Diamedix Corporation Due to Product...

The Issue: Product contained an incorrect substrate.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 1/4 in. Trocar with Single Drain Curved Trocar with Wound Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 1/4 in. Curved Trocar with Wound Drain Curved Trocar with Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· PhotoMedex, Inc.

Recalled Item: Iamin Moist Dressing and the Iamin Hydrating Gel: intended to Recalled by...

The Issue: The labeling for the Iamin family of medical devices (e.g. printed and...

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

Class II — Potential Health HazardOngoing
DrugMarch 26, 2015· Actavis Laboratories, FL, Inc.

Recalled Item: Cartia XT (diltiazem HCl extended-release capsules Recalled by Actavis...

The Issue: Presence of Foreign Substance; fine residue or dust identified as aluminum...

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

Class III — Low RiskOngoing
Refund
DrugMarch 26, 2015· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Fexofenadine Hydrochloride Tablets Recalled by Mylan Institutional, Inc....

The Issue: Failed Impurities/Degradation Specifications: the manufacturer, recalled...

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

Class III — Low RiskOngoing
Refund
DrugMarch 25, 2015· Heritage Pharmaceuticals, Inc.

Recalled Item: GLIPIZIDE and METFORMIN HYDROCHLORIDE Tablets Recalled by Heritage...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2015· Qualitest Pharmaceuticals

Recalled Item: PROMETHAZINE VC WITH CODEINE SYRUP Recalled by Qualitest Pharmaceuticals Due...

The Issue: Failed Impurities/Degradation Specifications: A stability lot was out of...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 25, 2015· Nidek Inc

Recalled Item: Dual Delivery 4DD-1 of GYC-1000 Green Laser Photocoagulator system GYC4DD-1:...

The Issue: Accessories to the GYC-1000 laser were missing Laser Aperture labels.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Universal Charger Product Usage: The Stryker Universal Battery Charger is...

The Issue: The Stryker Universal Battery Charger is not transmitting usage data to the...

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

Class III — Low RiskOngoing
Medical DeviceMarch 25, 2015· Nidek Inc

Recalled Item: Endophotocoagulation Delivery 4EP-1 of GYC-1000 Green Laser Photocoagulator...

The Issue: Accessories to the GYC-1000 laser were missing Laser Aperture labels.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2015· Lumenis Limited

Recalled Item: Light Sheer Desire Diode Laser System with XC Handpiece Accessory options....

The Issue: Device software treatment preset parameters for the XC treatment handpiece...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2015· SenTec AG

Recalled Item: Sentec Recalled by SenTec AG Due to SenTec is voluntarily replacing V-Sign...

The Issue: SenTec is voluntarily replacing V-Sign Sensors 2 due to pre-mature...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2015· Laax, Inc.

Recalled Item: TIGERPAW System II Recalled by Laax, Inc. Due to Increase of field reports...

The Issue: Increase of field reports involving issues with the TIGERPAW System II...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 25, 2015· Laax, Inc.

Recalled Item: TIGERPAW System II Recalled by Laax, Inc. Due to Increase of field reports...

The Issue: Increase of field reports involving issues with the TIGERPAW System II...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 25, 2015· CSA Medical

Recalled Item: CSA Medical truFreeze Console- Cryosurgical Unit Cryogenic Surgical Device...

The Issue: TruFreeze Console caused a higher rate of liquid nitrogen (cryogen) to be...

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

Class II — Potential Health HazardOngoing
DrugMarch 24, 2015· Nomax Inc

Recalled Item: Rose Bengal GloStrips (rose bengal) Ophthalmic Strips USP Recalled by Nomax...

The Issue: Failed Content Uniformity Specifications: The product may not meet finished...

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

Class III — Low RiskOngoing
Refund
DrugMarch 24, 2015· Nomax Inc

Recalled Item: Fluorescein Sodium Ophthalmic Strips USP Recalled by Nomax Inc Due to Failed...

The Issue: Failed Content Uniformity Specifications: The product may not meet finished...

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

Class III — Low RiskOngoing
Refund
DrugMarch 24, 2015· Nomax Inc

Recalled Item: Fluorescein Sodium Ophthalmic Strips USP Recalled by Nomax Inc Due to Failed...

The Issue: Failed Content Uniformity Specifications: The product may not meet finished...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 24, 2015· Hamilton Medical, Inc.

Recalled Item: Hamilton-G5 Ventilators with software versions V2.40/2.41 Catalog numbers...

The Issue: Customer reports that the ventilator display can freeze. Ventilation...

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

Class II — Potential Health HazardOngoing