Recalls published in May 2026
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in May 2026, newest first.
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Class II · 5 months ago
Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product recall: A software defect in which a low-priority file I/O check blocks
A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs)…
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Class II · 5 months ago
Stryker Sustainability Solutions Daig Livewire Steerable, Product Number 401905 recall: Incomplete seals on sterile product
Incomplete seals on sterile product
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Class I · 5 months ago
Arrow International, LLC NextStep Antegrade Chronic Hemodialysis Catheter recall: 16F dual-valved splittable sheath introducer
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer…
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Class II · 5 months ago
Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product recall: A software defect in which a low-priority file I/O check blocks
A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs)…
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Class II · 5 months ago
Quidel Corporation QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens recall: Product has the potential for false positive results
Product has the potential for false positive results
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Class I · 5 months ago
Arrow Edge Hemodialysis Catheterization Product recall: 16F dual-valved splittable sheath introducer
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer…
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Class II · 5 months ago
Stryker Corporation Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code recall: Due to nonconforming products being inadvertently distributed
Due to nonconforming products being inadvertently distributed.
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Class I · 5 months ago
Arrow-Clark VectorFlow Antegrade Chronic Hemodialysis Catheter: REF recall: 16F dual-valved splittable sheath introducer
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer…
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Class II · 5 months ago
GE Medical Systems, LLC Revolution Apex Select, X-ray Computed Tomography recall: GE HealthCare has become aware of a potential security vulnerability
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart…
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Class II · 5 months ago
On-X Mitral Heart Valve with Conform-X Sewing Ring, Model: ONXMC-25/33 recall: Heart valves were released and distributed before all required testing
Heart valves were released and distributed before all required testing was complete, so it cannot be confirmed that they meet all release…
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Class I · 5 months ago
Windstone Medical Packaging, Inc. Custom Convenience Kit containing recalled Medline recall: Affected kits contain Medline Namic RA Syringes
Affected kits contain Medline Namic RA Syringes, which are recalled by their manufacturer due to risk of syringe rotating adapter unwinding during…
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Class II · 5 months ago
Stryker Sustainability Solutions BARD Dynamic Tip Steerable, Product Number 200344 recall: Incomplete seals on sterile product
Incomplete seals on sterile product
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Class II · 5 months ago
Stryker Sustainability Solutions Daig Livewire Steerable, Product Number 401915 recall: Incomplete seals on sterile product
Incomplete seals on sterile product
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Class II · 5 months ago
Stryker Sustainability Solutions Daig Livewire Steerable, Product Number 401581 recall: Incomplete seals on sterile product
Incomplete seals on sterile product
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Class II · 5 months ago
Stryker Sustainability Solutions BARD EP XT Decapolar Steerable, Product Number 201007 recall: Incomplete seals on sterile product
Incomplete seals on sterile product
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Class II · 5 months ago
Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer recall: Software issue: When programming the SynchroMed Pump with the A810 CP App
Software issue: When programming the SynchroMed Pump with the A810 CP App in Flex Infusion Mode, the infusion steps should automatically be arranged…
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Class I · 5 months ago
Medline medical convenience kits, containing Namic Manifold recall: Medline has identified the presence of particulate within the fluid path
Medline has identified the presence of particulate within the fluid path of the Manifolds.
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Class I · 5 months ago
Namic Preceptor Manifold, custom, Medline Product Number/SKU 64037107 recall: Medline has identified the presence of particulate within the fluid path
Medline has identified the presence of particulate within the fluid path of the Manifolds.
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Class II · 5 months ago
GE Medical Systems, LLC Revolution Ascend, computed tomography recall: GE HealthCare has become aware of a potential security vulnerability
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart…
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Class II · 5 months ago
Stryker Sustainability Solutions Daig Livewire Steerable, Product Number 401904 recall: Incomplete seals on sterile product
Incomplete seals on sterile product
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Class I · 5 months ago
Rolls of label stock used with the Omnicell i.v.Station. 1 recall: Potential for mislabeled syringe produced by the i.v.STATION device
Potential for mislabeled syringe produced by the i.v.STATION device.
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Class II · 5 months ago
Hologic, Inc Selenia Dimensions Mammography Systems. Model Numbers recall: Complaints have been received of systems developing loose, missing
Complaints have been received of systems developing loose, missing, or broken internal bolts over time.
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Class II · 5 months ago
Stryker Sustainability Solutions BARD Dynamic Deca Steerable, Product Number 201101 recall: Incomplete seals on sterile product
Incomplete seals on sterile product
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Class II · 5 months ago
Djo, LLC Brand Name: Donjoy Product Name: Iceman W/,Univ,Loop,NS,EH Model/ recall: Due to broken connector which may result in a temporary interruption
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.