State

Wyoming product recalls

72,907 recalls have nationwide distribution and so reach Wyoming. 3,219 additional recalls listed Wyoming specifically in their distribution scope.

What the numbers show

Total: 3,219
Critical: 762
Severe: 543
Most recent: 2026-09-02

Of the 3,219 recalls naming Wyoming we have scored against our rubric, 762 (24%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 543 (17%) are Severe.

Which agencies issued them

These figures cover only the 3,219 recalls whose distribution notice names Wyoming specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

851–875 of 76126

SevereFDA (Devices)·Z-2548-2026·2026-07-08
Hillrom VOLARA System P.CIRCUIT KIT Medical Device Recall for Oxygen Drop Risk
Baxter Healthcare is recalling the Hillrom VOLARA System P.CIRCUIT KIT (Model REF M08085) due to reports of air and medication leakage from the nebulizer cup, which can cause oxygen level drops and reduce treatment effectiveness.
Product
Hillrom VOLARA System P.CIRCUIT KIT (Single Patient Use Circuit), Model/Catalog Number REF M08085; Oscillation Lung Expansion Therapy, positive pressure breathing device
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0659-2026·2026-07-08
Lidocaine Hydrochloride Injection Recalled for Sterility Assurance
Asclemed USA Inc. is recalling Lidocaine Hydrochloride Injection USP, 1% (10 mg/mL) in 5 mL single dose ampules nationwide due to lack of assurance of sterility. The affected lots have expiration dates of 11/30/2026 and 04/30/2028.
Product
LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE ANHYDROUS)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·26V441000·2026-07-08
BMW Recalls 29,119 Vehicles Due to Starter Relay Fire Risk
BMW is recalling 29,119 vehicles because a corroded starter relay may overheat and short circuit, increasing the risk of a fire.
Product
BMW — BMW 530E XDRIVE IPERFORMANCE, 740LE XDRIVE IPERFORMANCE, 530E IPERFORMANCE, 330E IPERFORMANCE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0651-2026·2026-07-08
ChloraPrep One-Step Applicators Recalled Due to Sterility Assurance Loss
CareFusion 213, LLC is recalling ChloraPrep One-Step chlorhexidine gluconate and isopropyl alcohol applicators distributed nationwide because unsterilized units intended for further processing were distributed through the wrong channels.
Product
CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·26V437000·2026-07-08
2026 Toyota Grand Highlander Hybrid rear axle carrier structural defect
Toyota is recalling certain 2026 Grand Highlander Hybrid and related models because the rear axle carriers may have insufficient material strength and could break, causing loss of vehicle control and increasing crash risk.
Product
LEXUS — LEXUS, TOYOTA TX PLUG-IN HYBRID, TX HYBRID, TX, GRAND HIGHLANDER HYBRID
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0645-2026·2026-07-08
ChloraPrep One-Step Applicators Recalled Due to Sterility Assurance Failure
CareFusion 213, LLC is recalling ChloraPrep One-Step applicators nationwide because unsterilized units intended for further processing were distributed to customers outside the intended distribution channel, lacking sterility assurance.
Product
CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0692-2026·2026-07-08
Revitaderm Wound Care Gel recalled for microbial contamination
Revitaderm Wound Care Gel has been recalled due to microbial contamination with Lysinibacillus fusiformis and other Bacillus species. The product was distributed nationwide and consumers should stop using it.
Product
Revitaderm Wound Care Gel, Benzalkonium Chloride 0.1%, packaged in 1.0 FL OZ (37 mL) bottle, shorter twist cap, Manufactured By: Blaine Labs, Inc. 11037 Lockport Place Santa Fe Springs, CA 90670, NDC 63347-120-02.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0648-2026·2026-07-08
ChloraPrep One-Step Antiseptic Applicators recalled for lack of sterility assurance
CareFusion is recalling ChloraPrep One-Step antiseptic applicators because unsterilized units intended for further processing were distributed outside the intended channel, creating a sterility assurance gap.
Product
CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2615-2026·2026-07-08
Reprocessed Electrophysiology Catheters Recalled for Residual Particles
Medline Industries is recalling reprocessed electrophysiology and ultrasound catheters with residual particles that may cause inflammation, infection, or blood clots if contacted with blood or the heart.
Product
Reprocessed Electrophysiology Catheters and Ultrasound Catheters Item no. 401206RH, St. Jude Medical Response" Diagnostic Electrophysiology Catheter 4 Elec. 10mm; Item no. 401305RH, St. Jude Medical Response" Diagnostic Electrophysiology Catheter 10 Elec. 2-5-2mm.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2612-2026·2026-07-08
Medline Convenience Kits with Recalled Swan-Ganz Catheters
Medline Convenience kits containing recalled Swan-Ganz catheters may leak or break at the proximal injectate lumen hub, risking infection, medication loss, and blood loss.
Product
Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH PACK CTX DYNJ68530A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2647-2026·2026-07-08
RayCare 2024A SP4 Oncology System Beam Set Delivery Note Data Loss
RayCare 2024A SP4 oncology information system may lose data or fail to notify users when beam set delivery notes are modified simultaneously or updated during treatment sessions.
Product
RayCare 2024A SP4. Oncology Information Systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2643-2026·2026-07-08
ARTIS icono floor Medical Imaging System Detector Movement Loss Recall
Siemens Medical Solutions is recalling 30 units of the ARTIS icono floor (Model 11327700) due to potential loss of detector movement capability when adjusted to maximum or minimum height limits.
Product
ARTIS icono floor. Model Number: 11327700.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2638-2026·2026-07-08
Baxter Head Positioning Adapter May Loosen During Patient Positioning
Baxter Healthcare is recalling an Adapter for Head Positioning (Model 1739994) used on operating tables because it may become loose and unintentionally move during patient positioning.
Product
Adapter for Head Positioning, Model/Catalog Number: 1739994, when used in conjunction with the side rails of the Upper Back Section H V U component (product code 1909813) on Baxter operating tables
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2613-2026·2026-07-08
Medline Convenience Kits with Recalled Swan-Ganz Catheters
Medline Convenience kits containing Swan-Ganz catheters recalled by Becton Dickinson are being recalled due to leaks and breakage of the proximal injectate lumen hub, which may result in infection, medication loss, or blood loss.
Product
Medline Convenience kits containing recalled Swan-Ganz Catheters CABG A CDS CDS982269K CDS982269L CDS982269M CDS982269N CARDIAC MAJOR DYNJ901328D DYNJ901328F HEART A DYNJ903465F DYNJ903465G HEART TRAY-VASCULAR DYNJ907857 DYNJ907857A DYNJ90
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2618-2026·2026-07-08
Medacta Short Monobloc Stem Broaches Surgical Instruments Shoulder Implant
Medacta USA is recalling Short Monobloc Stem Broaches used in shoulder replacement surgery due to positioning misalignment that may increase risk of fracture in the upper arm bone.
Product
Short Monobloc Stem Broaches, Size/REF: 7/04.01.10.0970, 8/04.01.10.0971, 9/04.01.10.0972, 10/04.01.10.0973, 11/04.01.10.0974, 12/04.01.10.0975, 13/04.01.10.0976, 14/04.01.10.0977, 15/04.01.10.0978, 16/04.01.10.0979 Part of Medacta Shoulder System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2606-2026·2026-07-08
Medline Convenience Kits with Swan-Ganz Catheters Recalled
Medline Industries is recalling convenience kits containing Swan-Ganz catheters due to leaks and breakage of the proximal injectate lumen hub, which may cause infection, medication loss, or blood loss.
Product
Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH PACK CTX DYNJ68530B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2639-2026·2026-07-08
Pilling Wecksorb Neurosponges Surgical Sponges Recalled for Endotoxin Contamination
Teleflex LLC is recalling Pilling Wecksorb Neurosponges and Neurosponge Strips due to out-of-specification or potentially out-of-specification endotoxin levels. The cotton surgical sponges are used in brain and spine surgery.
Product
Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips (Cotton) Model/Catalog Number: 200100 200101 200102 200103 200104 200105 200106 200108 200110 200112 200120 200121 200123 200131 Software V
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2646-2026·2026-07-08
RayCare 2024A SP1 Oncology Information System Software Recall
RayCare 2024A SP1 oncology software may lose data if beam set delivery notes are modified simultaneously or updated during treatment sessions, with users not notified of changes.
Product
RayCare 2024A SP1. Oncology Information Systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2628-2026·2026-07-08
CRE Pro Wireguided medical device sterile packaging breach recall
Boston Scientific Corporation is recalling the CRE Pro Wireguided 10-12mm 240cm device due to potential sterile breach of the pouches in which devices are packaged. The affected product has been distributed worldwide.
Product
CRE Pro Wireguided 10-12mm 240cm
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2629-2026·2026-07-08
Boston Scientific CRE Pro Wireguided 12-15mm Esophageal Stent Recall
Boston Scientific is recalling CRE Pro Wireguided 12-15mm 240cm esophageal stents due to a potential sterile breach in the device packaging. Affected units were distributed worldwide.
Product
CRE Pro Wireguided 12-15mm 240cm
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2642-2026·2026-07-08
ARTIS Icono Ceiling Model 11328100 Loss of Movement Capability Recall
Siemens Medical Solutions is recalling 119 units of the ARTIS icono ceiling (Model 11328100) due to potential loss of movement capability when the detector lift height is adjusted to its maximum or minimum limits.
Product
ARTIS icono ceiling. Model Number: 11328100.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2631-2026·2026-07-08
CRE Pro Wireguided esophageal stent device recalled for packaging sterility
Boston Scientific is recalling CRE Pro Wireguided 18-20mm 240cm esophageal stents due to potential sterile breach of product pouches. The breach could allow contamination of sterile devices.
Product
CRE Pro Wireguided 18-20mm 240cm
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V442000·2026-07-08
PETERBILT 579 Tractors Recalled for Air Brake Valve Installation
PACCAR is recalling certain 2026–2027 Peterbilt 579 and 2027 Kenworth T680 tractors with a potentially incorrectly installed trailer air connection quick release valve that can cause trailer instability after braking.
Product
KENWORTH — KENWORTH, PETERBILT T680, 579
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·H-1129-2026·2026-07-08
MorningStar Farms Buffalo Chik'n Nuggets recalled for potential plastic contamination
MorningStar Farms Buffalo Chik'n Nuggets (10.5 oz.) are being recalled due to potential contamination with plastic material. Affected products have Best If Used By dates of JUL 07 2027 and JUL 08 2027.
Product
MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein Vegan Nuggets, Net Wt. 10.5 oz. (298g), packaged in a resealable plastic bag with UPC 028989101105, packed 6 bags per case
Category
Food
Distribution
41 states
HighFDA (Devices)·Z-2625-2026·2026-07-08
IntelliCuff Portable Automatic Cuff Pressure Controller Recall
Hamilton Medical AG is recalling the IntelliCuff portable automatic cuff pressure controller due to a reported "Cuff System Leakage" error that may cause the motor to pump continuously and fail to maintain user-set cuff pressure.
Product
IntelliCuff, Portable automatic cuff pressure controller REF: 951001
Category
Medical Device
Distribution
Distributed nationwide