recall
saveKenvue Brands LLC recall (Cls II)
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TYLENOL, Acetaminophen, Extra Strength, 24 Caplets, 500mg each, distributed by: Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division, Fort Washington, PA 19034, NDC: 50580-378-04. — Reason: Defective Container — Status: Ongoing
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same company · ±60 days · 6
- approvalMACITENTAN — FDA approvalNov 5, 2025
- approvalSTELARA (USTEKINUMAB) — FDA approvalNov 3, 2025
- device pmaJohnson & Johnson Surgical Vision, Inc. — Healon EndoCoat PRO Sodium Hyaluronate Ophthalmic Viscoelastic Device (OVD), Healon Duet PRO II Dual Pack Sodium Hya (PMA supplement)Oct 28, 2025
- device pmaJohnson & Johnson Surgical Vision, Inc. — TECNIS Symfony Toric II OptiBlue Extended Range of Vision IOL with TECNIS Simplicity Delivery System, Models DXW150-375; (PMA supplement)Oct 24, 2025
- approvalMACITENTAN — FDA approvalDec 3, 2025
- device pmaVistakon, Johnson & Johnson Vision Products, Inc. — ACUVUE CONTACT LENS (PMA supplement)Dec 16, 2025
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top 7- tagOphthalmology26 co-mentions · 24 sources
- tagAdCom24 co-mentions · 24 sources
- tagPMA Approval24 co-mentions · 24 sources
- drugHYDROCODONE BITARTRATE AND ACETAMINOPHEN2 co-mentions · 1 sources
- tagRecall1 co-mentions · 1 sources
- drugOXYCODONE AND ACETAMINOPHEN1 co-mentions · 1 sources
- drugACETAMINOPHEN AND IBUPROFEN1 co-mentions · 1 sources
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