State

Wyoming product recalls

72,971 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 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4726–4750 of 76190

CriticalFDA (Food)·H-0125-2026·2025-10-29
Penne salad kits recalled over Listeria in recalled pasta ingredient
Albertsons Companies is recalling its store-made Smoked Mozzarella Penne Salad Kit because it contains a penne pasta ingredient recalled for Listeria monocytogenes.
Product
Smoked Mozzarella Penne Salad Kit, UPC 271876 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Carrs-Safeway, Eagle, and Safeway in AK.
Category
Food
Distribution
15 states
SevereNHTSA·25V737000·2025-10-29
Mazda CX-50 front suspension bolts may allow wheel detachment
Mazda is recalling certain 2025 CX-50 and CX-50 Hybrid vehicles because the front suspension fastener bolts may not be tightened properly, which can result in suspension component or wheel detachment.
Product
MAZDA — MAZDA CX-50, CX-50 HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0237-2026·2025-10-29
Blood culture systems recalled after service credentials were accessed by unauthorized actor
Becton Dickinson is recalling 1,086 BD BACTEC Blood Culture Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Product
BD BACTEC Blood Culture System, labeled as the following: 1. BACTEC 9120 System, Catalog Numbers: 445570, 445702. 2. INSTRUMENT BACTEC 9120 UNREPAIRED, Catalog Number: 44557008.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0210-2026·2025-10-29
Dual lumen stomach tubes recalled after anti-reflux valve breakage complaints
Cardinal Health is recalling all lots of Salem Sump dual lumen stomach tubes with anti-reflux valve after complaints of valve breakage due to excessive force during use.
Product
Salem Sump PVC Tubes: Product Code/Product Name: 266122 Salem Sump" Stomach Tube, Dual Lumen with Anti-Reflux Valve, 14 Fr/Ch (4.7 mm) 266130 Salem Sump" Stomach Tube, Dual Lumen with Anti-Reflux Valve, 16 Fr/Ch (5.3 mm) 266148 Salem Sump" Stomach Tube, Dual Lumen with Anti
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0115-2026·2025-10-29
Tovala frozen raw shrimp recalled over possible cesium 137 contamination
Southwind Foods is recalling Tovala branded frozen raw phosphate free shrimp in 5 oz bags because it may have been contaminated with Cesium-137.
Product
Tovala branded Frozen raw phosphate free shrimp; 5oz IQF bag UPC: 829944085788
Category
Food
Distribution
34 states
HighFDA (Drugs)·D-0036-2026·2025-10-29
Ketorolac injection vials recalled after glass particulate found in product
Aspiro Pharma is recalling Ketorolac Tromethamine Injection USP 60 mg/2 mL across several lots because of particulate matter identified as glass.
Product
KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0232-2026·2025-10-29
Insulin pumps recalled over software defect causing unexpected correction bolus
Tandem Diabetes Care is recalling 122,958 t:slim X2 and Mobi insulin pumps because a software defect when paired with a Dexcom G7 sensor may trigger an unexpected automatic correction bolus.
Product
t:slim X2 insulin pump with Interoperable Technology, Control-IQ+ technology, REF: 1014070, 1014071, 1014072, 1014073, and User Guide when using Dexcom G7 sensor; Tandem Mobi insulin pump with Interoperable Technology, Control-IQ+ technology, REF: 1014801, 1014811, 1014813, and
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0240-2026·2025-10-29
Veritor Connect software recalled after service credentials accessed by unauthorized actor
Becton Dickinson is recalling 38 BD Veritor Connect Software units after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Product
BD Veritor Connect Software, labeled as the following: 1. Veritor (NUC), Catalog Number: 444881. Transfers in vitro diagnostic results data on the BD Veritor Plus Analyzer to BD Synapsys.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0239-2026·2025-10-29
Automated microbiology systems recalled after service credentials were accessed by unauthorized actor
Becton Dickinson is recalling 4,283 BD Phoenix M50 Automated Microbiology Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Product
BD Phoenix M50 Instrument, labeled as the following: 1. BD Phoenix M50 Automated Microbiology System, Catalog Numbers: 443624, 44362409.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0238-2026·2025-10-29
BD MAX instruments recalled after service credentials accessed by unauthorized actor
Becton Dickinson is recalling 62 BD MAX System instruments after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Product
BD MAX System, for in vitro diagnostic (IVD) use, labeled as the following: 1. BD MAX System, BD MAX Instrument, Catalog Numbers: 44191609, 441927.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0114-2026·2025-10-29
Frozen cooked salad shrimp recalled over possible cesium 137 contamination
Southwind Foods is recalling Arctic Shores branded frozen cooked salad shrimp in 6 oz bags because it may have been contaminated with Cesium-137.
Product
Arctic Shores branded Frozen cooked salad shrimp; 6 oz bag UPC: 041130811685
Category
Food
Distribution
34 states
HighFDA (Drugs)·D-0097-2026·2025-10-29
Opdualag injection vials recalled from one lot over sterility assurance
Bristol-Myers Squibb is recalling 12,778 vials of Opdualag (nivolumab and relatlimab-rmbw) injection from one lot for lack of assurance of sterility.
Product
OPDUALAG — OPDUALAG (NIVOLUMAB AND RELATLIMAB-RMBW)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0215-2026·2025-10-29
Clinical analyzer modules recalled over dilution factor software anomaly affecting results
Beckman Coulter is recalling 160 DxC 500i Clinical Analyzer modules over a software anomaly that may not apply user-specified manual dilution factors, risking false low or high results.
Product
DxC 500i Clinical Analyzer Modules, DxC 500 AU Module w/ISE, DxC 500i (Part Number C63522), DxC 500 AU Module, DxC 500i (Part Number C63521), and Access 2 Module, DxC 500i (Part Number C13252)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0234-2026·2025-10-29
Prefilled saline flush syringes recalled over sodium chloride concentration shortfall
Medline is recalling 8,267,150 Excelsior Medical 0.9% Sodium Chloride prefilled flush syringes because a limited quantity may not meet the required concentration of sodium chloride.
Product
Excelsior Medical, 0.9% Sodium Chloride Injection, USP - 10 mL Fill, Item Number EMZ111240. Prefilled saline flush syringes
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0288-2026·2025-10-29
Defibrillator pad packs recalled over damaged pins disrupting electrical contact
HeartSine Technologies is recalling 1,291,165 Pad-Pak units because defibrillator pads may contain damaged pins that disrupt the mechanical fit and electrical contact.
Product
HeartSine Pad-Pak, REF: PAD-PAK-01, PAD-PAK-02, PAD-PAK-03, PAD-PAK-04, PAD-PAK-07, PAD-PAK-03J, PAD-PAK-04J
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0227-2026·2025-10-29
Bipolar hip heads recalled downstream after femoral components failed transit testing
Theken Companies is recalling 409 iNSitu Bipolar Hip System head assemblies in a downstream recall after BioPro femoral components failed transit testing, risking sterile barrier issues.
Product
iNSitu Bipolar Hip System, Bipolar head implant Part ID Description 10-22-0038 Bipolar Head Assembly, Size 38mm 10-22-0040 Bipolar Head Assembly, Size 40mm 10-22-0042 Bipolar Head Assembly, Size 42mm 10-22-0044 Bipolar Head Assembly, Size 44mm 10-22-0046 Bipolar Head Asse
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0231-2026·2025-10-29
ECG trunk cables recalled because improper module placement can cause overheating
GE is recalling 29,225 MAC VU360 acquisition trunk cables and module holders because incorrect placement of the module can wear the cable until it overheats in use.
Product
MAC VU360 Acquisition Trunk Cable and Module Holder, high performance, multichannel resting electrocardiograph, Model Number 2030360-001, Product Codes VU2 and VU4
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0211-2026·2025-10-29
Gastroduodenal sump tubes recalled after anti-reflux valve breakage complaints
Cardinal Health is recalling all lots of Salem Sump PVC gastroduodenal tubes after complaints of anti-reflux valve breakage due to excessive force during use.
Product
Salem Sump PVC Tubes: Product Code/Product Name: 1180264408 Salem Sump" PVC Gastroduodenal Tube, 10 Fr/Ch (3.3 mm) x 90 cm 1180264416 Salem Sump" PVC Gastroduodenal Tube, 12 Fr/Ch (4.0 mm) x 114 cm 1180264424 Salem Sump" PVC Gastroduodenal Tube, 14 Fr/Ch (4.7 mm) x 114 cm
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0207-2026·2025-10-29
PVC stomach tubes recalled after anti-reflux valve breakage complaints
Cardinal Health is recalling all lots of Salem Sump dual lumen stomach tubes after complaints of anti-reflux valve breakage due to excessive force during use.
Product
Salem Sump PVC Tubes: Product Code/Product Name: 264929 Salem Sump" Stomach Tube, Dual Lumen, 12 Fr/Ch (4.0 mm) 264945 Salem Sump" Stomach Tube, Dual Lumen, 14 Fr/Ch (4.7 mm) 264960 Salem Sump" Stomach Tube, Dual Lumen, 16 Fr/Ch (5.3 mm) 264986 Salem Sump" Stomach Tube, Du
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0206-2026·2025-10-29
ENFit sump tubes recalled after anti-reflux valve breakage complaints
Cardinal Health is recalling all lots of ENFit Salem Sump PVC tubes after complaints of anti-reflux valve breakage due to excessive force during use.
Product
Salem Sump PVC Tubes: Product Code/Product Name: 8888264911E ENFit" SALEM SUMP" PVC TUBE 10FR 36IN 8888264929E ENFit" SALEM SUMP" PVC TUBE 12FR 48IN 8888264945E ENFit" SALEM SUMP" PVC TUBE 14FR 48IN 8888264960E ENFit" Salem Sump" PVC Tube 16Fr 48IN 8888264986E ENFit" SA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0113-2026·2025-10-29
Frozen raw shrimp recalled across four brands over cesium 137 contamination
Southwind Foods is recalling frozen raw shrimp sold under the Arctic Shores, Best Yet, Great American and Master Catch brands because it may have been contaminated with Cesium-137.
Product
Arctic Shores; Best Yet; Great American; Master Catch branded Frozen Raw shrimp; 2lbs; 1lbs; UPC: 041130810923; 041512179471; 041130810978; 041130811029; 011110641182; 829944010636; 041130811333; 041130810916; 041130812460; 041130810824; 829944012463; 829944012012; 829944004079
Category
Food
Distribution
34 states
HighFDA (Devices)·Z-0208-2026·2025-10-29
Silicone stomach tubes recalled after anti-reflux valve breakage complaints
Cardinal Health is recalling all lots of Salem Sump silicone dual lumen stomach tubes after complaints of anti-reflux valve breakage due to excessive force during use.
Product
Salem Sump PVC Tubes: Product Code/Product Name: 8888265108 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 10 Fr/Ch (3.3 mm), 36 (91 cm) 8888265116 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 12 Fr/Ch (4.0 mm), 48 (122 cm) 8888265124 Salem
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0216-2026·2025-10-29
Immunoassay analyzers recalled over dilution factor anomaly affecting patient results
Beckman Coulter is recalling 571 DxI 9000 Access Immunoassay Analyzers over a software anomaly that may not apply user-specified manual dilution factors, risking false low or high results.
Product
DxI 9000 Access Immunoassay Analyzer, Part Number C11137
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0209-2026·2025-10-29
Gastric sump anti-reflux valves recalled after breakage complaints from excessive force
Cardinal Health is recalling all lots of Salem Sump Anti-Reflux Valves after complaints of valve breakage due to excessive force during use, and is providing additional guidance for use.
Product
Salem Sump PVC Tubes: Product Code/Product Name: 266197 Salem Sump" Anti-Reflux Valve CE Marked 8888266197 Salem Sump" Anti-Reflux Valve
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0236-2026·2025-10-29
BACTEC FX instruments recalled after service credentials accessed by unauthorized actor
Becton Dickinson is recalling 177 BD BACTEC Blood Culture System instruments after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Product
BD BACTEC Blood Culture System, labeled as the following: 1. BD BACTEC FX, Instrument Top, Packaged, Catalog Number: 44138509. 2. Instrument Top Remanufactured Bactec Fx, Catalog Number: 441676. 3. BACTEC 9240 System, Catalog Number: 445569. 4. BD BACTEC FX40 Instrum
Category
Medical Device
Distribution
Distributed nationwide