Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,367 recalls have been distributed to Wyoming in the last 12 months.
Showing 28141–28160 of 48,219 recalls
Recalled Item: Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R)...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arterial Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) ARROWg+ard Blue You-Blend Two-Lumen Hemodialysis Catheterization Kit for...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) ARROWg+ard Blue MAC Two-Lumen Central Venous Access Kit 2) Recalled by...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
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.
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.
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.
Recalled Item: AMLODIPINE BESYLATE TABLET Recalled by Ascend Laboratories LLC Due to...
The Issue: PRESENCE OF FOREIGN TABLETS/CAPSULES: A 2.5 mg Amlodipine Besylate tablet...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GEC LX Laxoplex 60 capsules Dietary Supplement Recalled by Genetic Edge...
The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
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.
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.
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.
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.
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.
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.
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.
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.