Recalls published in February 2026
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in February 2026, newest first.
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Class II · 9 months ago
Medline medical procedure convenience kits labeled as: 1) Rr-Gyn recall: Medline kits were manufactured and distributed containing MASTISOL liquid
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing…
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Class II · 9 months ago
Philips North America Ingenia Elition S. Product Code : 781357, 782106 recall: The potential for stiffness value errors when viewing exported MR
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication…
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Class II · 9 months ago
Medline medical procedure convenience kits labeled as: 1) Depaul Basic recall: Medline kits were manufactured and distributed containing MASTISOL liquid
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing…
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Class II · 9 months ago
Medline medical procedure convenience kits labeled as: 1) Cath LAB recall: Medline kits were manufactured and distributed containing MASTISOL liquid
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing…
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Class II · 9 months ago
Philips North America Ingenia Ambition X. Product Code : 781356, 782109 recall: The potential for stiffness value errors when viewing exported MR
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication…
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Class II · 9 months ago
Philips North America SmartPath to dStream for XR and 3.0T. Product Code : 781270. MR recall: The potential for stiffness value errors when viewing exported MR
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication…
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Class II · 9 months ago
Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 5000TS recall: Device user interface (screen) may freeze or become unresponsive to touch
Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause…
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Class II · 9 months ago
Canon Medical System, USA, INC. Alphenix INFX-8000F recall: It has been discovered that there is a possibility that the fixing screws
It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of…
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Class II · 9 months ago
Medline medical procedure convenience kits labeled as: 1) C-Section recall: Medline kits were manufactured and distributed containing MASTISOL liquid
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing…
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Class II · 9 months ago
Philips North America Evolution Upgrade 3.0T. Product Code : 782143. MR systems recall: The potential for stiffness value errors when viewing exported MR
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication…
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Class II · 9 months ago
Gold Star Distribution Inc Toothbrushes, labeled as: Oral B Tooth Brush Shiny Clean recall: Potential exposure of rodents and rodent activity in the distribution center
Potential exposure of rodents and rodent activity in the distribution center.
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Class II · 9 months ago
Cerapedics, Inc. PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft recall: Incorrect expiration date
Incorrect expiration date
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Class II · 9 months ago
Philips North America Ingenia Elition X. Product Code : 781358, 782107 recall: The potential for stiffness value errors when viewing exported MR
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication…
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Class II · 9 months ago
Gold Star Distribution Inc Feminine hygiene products recall: Potential exposure of rodents and rodent activity in the distribution center
Potential exposure of rodents and rodent activity in the distribution center.
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Class II · 9 months ago
Aju Pharm Co., Ltd. Genesis Knotless Anchor recall: Reports of device failure, including anchor breakage, anchor bending
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
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Class II · 9 months ago
Cardinal Health 200, LLC Chest Drainage Units and Accessories: Product Code recall: The firm is updating the IFU to clarify the intended patient population
The firm is updating the IFU to clarify the intended patient population for the identified chest drainage units and accessories as adults, 18 years…
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Class II · 9 months ago
Philips North America Ingenia 3.0T CX. Product Code : 781271. MR systems with SW recall: The potential for stiffness value errors when viewing exported MR
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication…
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Class II · 9 months ago
Philips North America MR 7700. Product Code : 782120 recall: The potential for stiffness value errors when viewing exported MR
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication…
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Class II · 9 months ago
Philips North America Ingenia 3.0T. Product Code : 781342 recall: The potential for stiffness value errors when viewing exported MR
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication…
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Class II · 9 months ago
Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 3200TS recall: Device user interface (screen) may freeze or become unresponsive to touch
Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause…
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Class II · 9 months ago
Medline medical procedure convenience kits labeled as: 1) Drawer 1 recall: Medline kits were manufactured and distributed containing MASTISOL liquid
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing…
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Class II · 9 months ago
Medline medical procedure convenience kits labeled as: Head Shave-Latex recall: Medline kits were manufactured and distributed containing MASTISOL liquid
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing…
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Class II · 9 months ago
Medline medical procedure convenience kits labeled as: 1) Inpatient recall: Medline kits were manufactured and distributed containing MASTISOL liquid
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing…
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Class II · 9 months ago
Aju Pharm Co., Ltd. Fixone Hybrid Anchor recall: Reports of device failure, including anchor breakage, anchor bending
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.