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. 2,648 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
2,648 in last 12 months

Showing 96219640 of 29,298 recalls

Medical DeviceJune 2, 2021· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System Standard Cone Prox Body Recalled by...

The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System High Offset Cone Prox Body Recalled by...

The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System High Offset Cone Prox Body Recalled by...

The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System Standard Cone Prox Body Recalled by...

The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System High Offset Cone Prox Body Recalled by...

The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: ANCILLARY ADULT 140-DOSE CONVENIENCE KIT Recalled by Mckesson...

The Issue: Two unsuitable 3mL syringes with conventional needles for vaccine...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System Standard Cone Prox Body Recalled by...

The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System Standard Cone Prox Body Recalled by...

The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System Standard Cone Prox Body Recalled by...

The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System Standard Cone Prox Body Recalled by...

The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System Standard Cone Prox Body Recalled by...

The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System Standard Cone Prox Body Recalled by...

The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System High Offset Cone Prox Body Recalled by...

The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2021· Integra LifeSciences Corp.

Recalled Item: CODMAN RANEY SCALP CLIPS-Disposable cylindrical clips designed to provide...

The Issue: Packaging-pouches with wrinkles across the Tyvek side may compromise the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2021· Ossur Americas

Recalled Item: OSSUR MIAMI J SELECT COLLAR - Product Usage: is intended Recalled by Ossur...

The Issue: Due to insufficient column strength of the racks for all load conditions,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2021· Hill-Rom, Inc.

Recalled Item: Affinity Four Birthing Bed-used as a birthing bed for women Recalled by...

The Issue: Latch mechanism on the Lift-Off foot section of the Affinity Four Birthing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2021· Stryker GmbH

Recalled Item: Nail Insertion Sleeve Recalled by Stryker GmbH Due to The devices have a...

The Issue: The devices have a different inner diameter than the diameter specified on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2021· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: 3AA battery cradle (Part Number 045-001699-01) used with BeneVision TD60...

The Issue: Telepack may not power on when using the 3AA battery cradle.

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

Class III — Low RiskOngoing
Medical DeviceMay 27, 2021· Cytocell Ltd.

Recalled Item: Cytocell LPH019-A E2A (TCF3) Breakapart Probe- In Vitro Diagnostic Analyte...

The Issue: May show unexpected locus specific signals in addition to those at 19p13.3....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2021· Stryker GmbH

Recalled Item: Nail Insertion Sleeve Recalled by Stryker GmbH Due to The devices have a...

The Issue: The devices have a different inner diameter than the diameter specified on...

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

Class II — Potential Health HazardOngoing