Recalls distributed in Wyoming
These notices name Wyoming in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
1,195 stored notices name Wyoming, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Wyoming too — those are in the archive.
Reported Jun 17, 2020
Infant/Child Reduced Energy Defibrillation Electrodes, Part Number: 3202380-006, for use with LIFEPAK 1000…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2020
Gambro Cartridge Blood Set Prime Line - Product Usage: is intended for single use in a hemodialysis treatment using…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2020
Beckman Coulter Access Immunoassay Systems, Access Free T4 Thyroxine, REF 33880 (UDI:15099590225834) for use with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2020
OSTEOVATIONEX 2CC INJECT FORMULA. REF/UDI: 390-0002/00813845020009 - Product Usage: The product provides a bone void…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Osteomed, LLC
11 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 3, 2020
Epix latis GRASPER, 5 mm x 35 cm, REF C4130, Qty: 10, Sterile R, CE, Rx ONLY, UDI: (01)00607915110147
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Applied Medical Resources Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 13, 2020
R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496; REF/UDI: 257-1810D(01)10818788021493 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Epimed International
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 13, 2020
REF: AH7117 111" 10 Drop Admin Set w/2 Inj Sites, Rotating Luer, Sterile R, For Veterinary Use Only, (01) 1 0887709…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
10 more products in this recall
FDA (openFDA device enforcement)
Reported May 6, 2020
Lead diagnostic electrocardiograph under the following device names: ELI 10, ELI 350, ELI 150c, ELI 250c, ELI 230, ELI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Welch Allyn, Inc/mortara
9 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 15, 2020
LabPro Data Management System, UDI: 15099590676872 - Product Usage: The LabPro Data Management System is a Microsoft…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 15, 2020
BIOMET StageOne Hip Cement Spacer Mold with Insert, 48 MM, Silicone, Sterile, Item 431181.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
32 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 15, 2020
ABL800 FLEX, model number/UDI 393-800/0570 In Vitro testing of samples of whole blood for the parameters pH, pO2, pCO2,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Apr 15, 2020
ARTISTE MV System Model #8139789 with Digital LINAC Systems Control Console Software Versions 6, 7, 9, 13
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 15, 2020
PRIVATE SELECTION FROZEN BERRY MEDLEY in 16 oz. (10 bags per case) and 48 oz. bags (6 bags per case). UPC: 0001111079120
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Kroger Co.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 8, 2020
Sushi Ebi Cooked Butterfly Tail-On Whiteleg Shrimp; Tray +0.498 pounds; 20 individual trays per case Distributed by AFC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Fresh Concepts Corp.
FDA (openFDA food enforcement)
Reported Apr 8, 2020
Philips V60 Ventilators with Power Management PCBA part number 1055906
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Respironics California, LLC
FDA (openFDA device enforcement)
Reported Apr 8, 2020
Instructions for Use and Surgical Cleaning and Sterilization Protocol for: (1) Trilliant Surgical Tiger Cannulated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical, LLC
10 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 8, 2020
NATURAL GROCERS PEANUT CLUSTERS DK CHOCOLATE NON-GMO, 8 oz. (227g), packed in a plastic bag, UPC 000087562088, Packaged…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vitamin Cottage Natural Food Markets, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 1, 2020
1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter REF: 1709600, Air Guard,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2020
VNS Therapy Programmer, Model 3000 used with Models 103, 104, 105, 106, or 8103 VNS Therapy generators.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2020
Medline Stick Sponge Presaturated W/PVP REF DYND70288 DYND70288H 2/PK Expiration 06/30/2022.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 25, 2020
CME America BodyGuard Infusion Pump System, All models of BG 323, BG 121, BG 545, BG CV545, BG 575, BG CV575, and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CME America, LLC
FDA (openFDA device enforcement)
Reported Mar 25, 2020
IMMULITE 1000 Systems E2 Estradiol Catalog #: US: LKE21(D) and OUS: LKE21 - Product Usage: For in vitro diagnostic use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2020
Stonewall Kitchen, Ghost Pepper Salsa, Net Weight 454g (16oz), Ingredients: Tomatoes, Jalapeno Peppers, Onion, Tomato…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stonewall Kitchen, LLC
FDA (openFDA food enforcement)
Reported Mar 18, 2020
American Bounty brand Icing Mix Vanilla, Item #32595, in 5 lb. metallic pouches, 6 pouches per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tova Industries Inc.
21 more products in this recall
FDA (openFDA food enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.