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. 1,827 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,827 in last 12 months

Showing 3636136380 of 52,570 recalls

Medical DeviceFebruary 4, 2016· Bard Peripheral Vascular Inc

Recalled Item: Bard TruGuide Disposable Coaxial Biopsy Needle Product Usage: The TruGuide...

The Issue: Bard Peripheral Vascular, Inc. is recalling Bard TruGuide Disposable Coaxial...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare Diagnostics ADVIA Centaur Calibrator E- 6- Pack Catalog...

The Issue: ADVIA Centaur Systems Calibrator E Lot 42 and 43 Bias with the Testosterone...

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

Class II — Potential Health HazardOngoing
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Dried Sausage Sticks under the following...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Smoked Pepperoni under the following labels:...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Dried Sticks Hot under the following Recalled by...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Summer Sausage under the following labels:...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Goetburg Summer Sausage under the following...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Trail Bologna under the following labels:...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 3, 2016· Zimmer Spine, Inc.

Recalled Item: Virage OCT Spinal Fixation System. Intended to promote fusion of Recalled by...

The Issue: Zimmer Biomet Spine is initiating a Medical Device Correction regarding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2016· Medical Action Industries Inc

Recalled Item: PICC/CVC Secure Dressing Change kit Recalled by Medical Action Industries...

The Issue: Misbranding; Due to the presence of CHG in the Tegaderm PICC/CVC dressing...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2016· Stryker Medical Division of Stryker Corporation

Recalled Item: S3 MedSurg Bed Recalled by Stryker Medical Division of Stryker Corporation...

The Issue: CPU board failures cause fowler (backrest) electronic controls to stop working.

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

Class II — Potential Health HazardOngoing
DrugFebruary 2, 2016· Hospira Inc.

Recalled Item: Normosol-M and 5% Dextrose (multiple electrolytes and 5% dextrose) Injection...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Confirmed customer...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 2, 2016· Isomeric Pharmacy Solution, LLC

Recalled Item: Triamcinolone Diacetate Injectable Suspension Recalled by Isomeric Pharmacy...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: some vials may be...

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

Class III — Low RiskOngoing
Refund
FoodFebruary 1, 2016· Geneva Foods, LLC

Recalled Item: Lysander's All Natural Bourbon Flavor Rub Recalled by Geneva Foods, LLC Due...

The Issue: Product contains undeclared allergens soy and wheat. Also does not declare...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 1, 2016· Geneva Foods, LLC

Recalled Item: Lysander's All Natural Spicy Bourbon Flavor Rub Recalled by Geneva Foods,...

The Issue: Product contains undeclared allergens soy and wheat. Also does not declare...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 1, 2016· Geneva Foods, LLC

Recalled Item: Lysander's Premium Teriyaki Marinade Recalled by Geneva Foods, LLC Due to...

The Issue: Product contains undeclared allergens soy and wheat. Also does not declare...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 31, 2016· Merge Healthcare, Inc.

Recalled Item: RadSuite software. The firm name on the label is Merge Healthcare Recalled...

The Issue: Potential for RadSuite AV viewer to skip image slices when the user presses...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2016· Merge Healthcare, Inc.

Recalled Item: Merge OfficePACS software. The firm name on the label is Merge Healthcare...

The Issue: Potential data loss occurs as a result of product archiving not working...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: CADstream software. The firm name on the label is Merge Healthcare Recalled...

The Issue: The software was not presenting the PURE filter user interface message on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: Merge OfficePACS software. The firm name on the label is Merge Healthcare...

The Issue: Potential data loss occurs as a result of the software archiving not working...

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

Class II — Potential Health HazardOngoing