Recalls published in March 2026
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in March 2026, newest first.
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Class II · 8 months ago
Medline Convenience Kits: 1) NAIL KIT recall: Medline has identified that the manufacturer of the sterile saline wound wash
Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required…
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Class II · 8 months ago
Olympus Resection Sheath, 26 Fr. with Deflecting Obturator recall: Complaints of the ceramic tip of the resection sheath breaking have
Complaints of the ceramic tip of the resection sheath breaking have been received.
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Class II · 8 months ago
Medtronic Perfusion Systems Octopus Nuvo Tissue Stabilizer recall: During the manufacturing, Medtronic personnel identified an assembly issue
During the manufacturing, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached…
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Class II · 8 months ago
Olympus Resection Inner Sheath, for 26 Fr. Outer Sheath recall: Complaints of the ceramic tip of the resection sheath breaking have
Complaints of the ceramic tip of the resection sheath breaking have been received.
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Class II · 8 months ago
Olympus Inner Sheath recall: Complaints of the ceramic tip of the resection sheath breaking have
Complaints of the ceramic tip of the resection sheath breaking have been received.
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Class II · 8 months ago
Olympus Resection Sheath, 28 Fr. with Deflecting Obturator recall: Complaints of the ceramic tip of the resection sheath breaking have
Complaints of the ceramic tip of the resection sheath breaking have been received.
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Class II · 8 months ago
Olympus Inner Sheath recall: Complaints of the ceramic tip of the resection sheath breaking have
Complaints of the ceramic tip of the resection sheath breaking have been received.
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Class II · 8 months ago
Olympus Resection Sheath, 28 Fr recall: Complaints of the ceramic tip of the resection sheath breaking have
Complaints of the ceramic tip of the resection sheath breaking have been received.
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Class II · 8 months ago
Convenience kits used for dialysis maintenance Medline ADD A Cath recall: Affected lots may exhibit issues with the silicone seal on Tego Connectors
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal…
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Class II · 8 months ago
Olympus Inner Sheath, Long recall: Complaints of the ceramic tip of the resection sheath breaking have
Complaints of the ceramic tip of the resection sheath breaking have been received.
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Class II · 8 months ago
MRIMed Inc. MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL recall: Due to battery component overheating while charging resulting in melting
Due to battery component overheating while charging resulting in melting of internal components and causing smoke.
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Class II · 8 months ago
Olympus Resection Sheath, 24 Fr., with Deflecting Obturator recall: Complaints of the ceramic tip of the resection sheath breaking have
Complaints of the ceramic tip of the resection sheath breaking have been received.
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Class II · 8 months ago
Encore Medical, LP Brand Name: Reverse Shoulder Prosthesis Product Name: RSP Humeral recall: Knee and Humeral socket implants contain incorrect labeling
Knee and Humeral socket implants contain incorrect labeling.
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Class II · 8 months ago
Olympus Sheath, 10 Fr recall: Complaints of the ceramic tip of the resection sheath breaking have
Complaints of the ceramic tip of the resection sheath breaking have been received.
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Class II · 8 months ago
Convenience kits containing Tego Connectors Medline Dialysis Drsng Chng recall: Affected lots may exhibit issues with the silicone seal on Tego Connectors
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal…
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Class II · 8 months ago
Medline Kits containing Tego Connectors Medline Dialysis ON/OFF KIT SKU recall: Affected lots may exhibit issues with the silicone seal on Tego Connectors
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal…
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Class II · 8 months ago
Wizcure Pharmaa Private Limited CHNaO Fluorescein Sodium Ophthalmic Strips, USP 1mg recall: Lack of Assurance of Sterility: Products have not been manufactured
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
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Class II · 8 months ago
Agebox iKids-Growth capsules, 60-count bottles recall: Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren
Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren
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Class II · 8 months ago
Wizcure Pharmaa Private Limited Vista Meibo Tears Propylene Glycol 0.6% w/v Eye Drops recall: Lack of Assurance of Sterility: Products have not been manufactured
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
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Class II · 8 months ago
Agebox iKids-Growth , 60-count bottles, Manufactured Exclusively recall: Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren
Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren
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Class II · 8 months ago
Wizcure Pharmaa Private Limited Vista Gonio Eye Lubricant recall: Lack of Assurance of Sterility: Products have not been manufactured
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
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Class II · 8 months ago
Leo Pharma Inc Adbry, injection, 300 mg/2mL, Packaged as a) 1 x Single dose recall: Lack of Assurance of Sterility: due to the presence of particulate matter
Lack of Assurance of Sterility: due to the presence of particulate matter in one unit from the lot, which lab tests have identified as wool fiber.
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Class II · 8 months ago
Wizcure Pharmaa Private Limited Vista Gel Hypromellose USP 0.3% w/v recall: Lack of Assurance of Sterility: Products have not been manufactured
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
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Class II · 8 months ago
AvKARE Amantadine HCl, Capsules, UPS, 100 mg, 50 Capsules unit dose recall: Failed Dissolution Specifications: This recall has been initiated
Failed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution.