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. 1,002 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,002 in last 12 months

Showing 30481–30500 of 52,570 recalls

DrugMay 8, 2017· Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

Recalled Item: HYDROCORTISONE LOTION Recalled by Vintage Pharmaceuticals LLC, DBA Qualitest...

The Issue: Superpotent Drug: above specification for the assay.

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 8, 2017· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. Merge PACS (Picture Archiving Communication System) is...

The Issue: When cut lines are shown on an image, the lines may go from being vertical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2017· Sterilmed Inc

Recalled Item: Electrophysiology catheter cables are designed as electrode cables with a...

The Issue: Sterilmed is recalling all lots of specific product codes of unexpired...

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

Class II — Potential Health HazardOngoing
FoodMay 8, 2017· RB Manufacturing LLC

Recalled Item: Schiff Move Free Advanced Plus MSM & Vitamin D3 with Glucosamine +...

The Issue: RB Manufacturing is recalling Move Free Advance Tablets due to incorrect...

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

Class III — Low RiskOngoing
Refund
FoodMay 8, 2017· Fourth Street Barbeque, Inc.

Recalled Item: Pick 5 Chicken & Waffle Sandwich Recalled by Fourth Street Barbeque, Inc....

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 8, 2017· Zimmer Biomet, Inc.

Recalled Item: Reusable instruments in the Knee Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Durability characteristics of reusable instruments were not established

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2017· Merge Healthcare, Inc.

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

The Issue: Merge PACS did not show unviewed images when the last view was skipped....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: HHV-8 (13810) Recalled by Cell Marque Corporation Due to Cell Marque has...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: SV40 (MRQ-4) 0.5 ml catalog number 351 M-15. Microbiology - Recalled by Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Estrogen Receptor (SP1) 7.0 mL Catalog number 249R-18 Recalled by Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: CD117 Recalled by Cell Marque Corporation Due to Cell Marque has determined...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Adenovirus (20/11 & 2/6) Recalled by Cell Marque Corporation Due to Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Herpes Simplex Virus II 0.5 ml catalog number 362A-15 7.0 Recalled by Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Her2/Neu (EP3) Recalled by Cell Marque Corporation Due to Cell Marque has...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Herpes Simplex Virus I Recalled by Cell Marque Corporation Due to Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Alphatec Spine, Inc.

Recalled Item: Arsenal Spinal Fixation System Recalled by Alphatec Spine, Inc. Due to...

The Issue: Alphatec Spine is recalling the Arsenal Spinal Fixation System Set Screw due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Varicella Zoster Virus 7.0 ml catalog number 364M-18 Microbiology - Recalled...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: H. pylori (polyclonal} 1.0 mL Catalog number 215A-76 Recalled by Cell Marque...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Innovasis, Inc

Recalled Item: Opteryx Variable Rescue Screw Recalled by Innovasis, Inc Due to Opteryx...

The Issue: Opteryx Variable Rescue Screws are engraved with incorrect (larger) size (16...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Her2/Neu (c-erbB-2) (CB-1 1) Recalled by Cell Marque Corporation Due to Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing