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 2350123520 of 52,570 recalls

Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill for 3.5mm screw Recalled by Zimmer GmbH Due to An investigation...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: CBS 4.0 countersink Recalled by Zimmer GmbH Due to An investigation...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Compass Health Brands (Corporate Office)

Recalled Item: MediPress pneumatic compression system Recalled by Compass Health Brands...

The Issue: Product design change did not receive proper premarket clearance and lacks a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Compass Health Brands (Corporate Office)

Recalled Item: MediPress pneumatic compression system Full Leg (Short)-Segmental Gradient...

The Issue: Product design change did not receive proper premarket clearance and lacks a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Compass Health Brands (Corporate Office)

Recalled Item: MediPress pneumatic compression system Full Leg (Medium)-Segmental Gradient...

The Issue: Product design change did not receive proper premarket clearance and lacks a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Compass Health Brands (Corporate Office)

Recalled Item: MediPress pneumatic compression system Full Leg (Long)-Segmental Gradient...

The Issue: Product design change did not receive proper premarket clearance and lacks a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Compass Health Brands (Corporate Office)

Recalled Item: MediPress pneumatic compression system Full Arm (Short)-Segmental Gradient...

The Issue: Product design change did not receive proper premarket clearance and lacks a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Compass Health Brands (Corporate Office)

Recalled Item: MediPress pneumatic compression system Full Arm (Medium)-Segmental Gradient...

The Issue: Product design change did not receive proper premarket clearance and lacks a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· DePuy Spine, Inc.

Recalled Item: Concorde Lift Recalled by DePuy Spine, Inc. Due to A complaint trend was...

The Issue: A complaint trend was observed for post-operative loss of height and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· DePuy Spine, Inc.

Recalled Item: Concorde Lift Recalled by DePuy Spine, Inc. Due to A complaint trend was...

The Issue: A complaint trend was observed for post-operative loss of height and...

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

Class II — Potential Health HazardOngoing
DrugApril 5, 2019· Brian P. Richardson

Recalled Item: Kopi Jantan Tradisional Natural Herbs Coffee Recalled by Brian P. Richardson...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to be...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 5, 2019· Abbott Gmbh & Co. KG

Recalled Item: Alinity i Processing Module Recalled by Abbott Gmbh & Co. KG Due to...

The Issue: Potential loose cable connections on the reagent cooler, which could result...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2019· Advanced Bionics, LLC

Recalled Item: SoundWave Professional Suite Software 3.2 Recalled by Advanced Bionics, LLC...

The Issue: The manufacturer received complaints that customers were attempting to...

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

Class III — Low RiskOngoing
Medical DeviceApril 4, 2019· Roche Diagnostics Corporation

Recalled Item: cobas p 501 post-analytical units Recalled by Roche Diagnostics Corporation...

The Issue: There is a potential for the tray input flap on the post analytical units to...

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

Class III — Low RiskOngoing
Medical DeviceApril 4, 2019· Roche Diagnostics Corporation

Recalled Item: cobas p 701 post-analytical units Recalled by Roche Diagnostics Corporation...

The Issue: There is a potential for the tray input flap on the post analytical units to...

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

Class III — Low RiskOngoing
FoodApril 3, 2019· ConAgra Foods, INc.

Recalled Item: Hunts Tomato Paste No Salt Added 6 ounce cans Recalled by ConAgra Foods,...

The Issue: Mold. This situation is due to potential damage to the cans.

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

Class II — Potential Health HazardOngoing
Refund