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. 1,894 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,894 in last 12 months

Showing 2632126340 of 29,298 recalls

Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Sekisui Diagnostics LLC

Recalled Item: Product Name: OSOM C. Difficile Toxin A/B Test Catalog Numbers: Recalled by...

The Issue: Sekisuki Diagnostics has issued a Product Correction for certain lot numbers...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential safety issue...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences EMBOL-X Glide Protection System Recalled by Edwards...

The Issue: Edwards Lifesciences is recalling certain lots of EMBOL-X Glide Protection...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2013· CooperSurgical, Inc. D.B.A. Lone Star Medical Products

Recalled Item: Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Recalled by CooperSurgical,...

The Issue: CooperSurgical is recalling two lots of 900-863 because the wrong package...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2013· Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical

Recalled Item: NX3 Try-In Gel. The product is used as a tooth shade resin material....

The Issue: Kerr Corporation is voluntarily recalling one lot of NX3 Try-In Gel, because...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2013· Southern Implants, Inc

Recalled Item: Tri-Nex Healing Abutment Recalled by Southern Implants, Inc Due to Southern...

The Issue: Southern Implants is recalling the Tri-Nex healing abutment because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2013· Mesa Laboratories, Inc.

Recalled Item: pH 7.0 Buffer Solution Pint and Quart Bottles Recalled by Mesa Laboratories,...

The Issue: Mesa Laboratories, Inc. is recalling certain lots of pH 7.0 Buffer Solution...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2013· Beckman Coulter Inc.

Recalled Item: Access 2 Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is recalling the Access 2 Immunoassay System because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2013· Maquet Medical Systems USA

Recalled Item: MAQUET Getinge Group CARDIOHELP Base Unit .7999 .8012 Recalled by Maquet...

The Issue: It has come to the attention of MAQUET that in certain rare instances, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2013· Leica Microsystems, Inc.

Recalled Item: Leica Ceiling Mount MSF-1 for use with M841 and M501 Recalled by Leica...

The Issue: The ceiling mount supplier encountered an event in which the drive screw in...

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

Class II — Potential Health HazardOngoing