State
73,817 recalls have nationwide distribution and so reach New York. 12,956 additional recalls listed New York specifically in their distribution scope.
Of the 12,956 recalls naming New York we have scored against our rubric, 1,508 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,702 (29%) are Severe.
Which agencies issued them
These figures cover only the 12,956 recalls whose distribution notice names New York specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
The FDA is recalling ZHANSHENG WEIGE CHAOYUE XILISHI tablets because they contain sildenafil, an unapproved drug for which safety and efficacy have not been established.
Medline Industries is recalling I&D Tray Kits because the Povidone-Iodine prep pads contain less iodine than the label claims.
Medline Industries is recalling sterile Povidone-Iodine prep pads because the iodine content is below the labeled 0.85% claim.
Medline Industries is recalling Circumcision Tray Kits because the iodine concentration in the prep pads is below the labeled claim.
A&H Focal Inc. is recalling DADIYONGSHI XIANGGANGTIANLONGSHENGWU tablets because they contain sildenafil, an unapproved drug for erectile dysfunction.
Medline Industries is recalling CNTRL Line Removal Kit Scripps because the iodine content is below the label claim.
Medline Industries is recalling Suture Removal Kits because the iodine concentration is below the label claim of 0.85%.
Medline Industries is recalling Suture Removal Trays because the Povidone-Iodine prep pads contain less iodine than the label claims.
A&H Focal Inc. is recalling Hard Ten Days capsules because they contain sildenafil, an unapproved drug for which safety and efficacy have not been established.
A&H Focal Inc. is recalling MACA gold tablets sold in New York and New Jersey because they contain sildenafil, an unapproved drug.
Medline Industries is recalling Abdominal Surgery II Packs because the iodine content in the prep pads is below the label claim.
Medline Industries is recalling Skin Stapler RMVR trays because the iodine concentration in the prep pads is below the labeled claim.
Medline is recalling Incision and Drainage Trays because the Povidone-Iodine prep pads contain less iodine than labeled.
Medline Industries is recalling Vitrectomy CDS Packs because the iodine concentration is below the label claim of 0.85%.
Medline Industries is recalling Debridement Trays because the iodine concentration in the prep pads is below the label claim.
Medline Industries is recalling Suture Removal Trays because the iodine content in the prep pads is below the labeled claim.
Medline Industries is recalling sterile Povidone-Iodine prep pads because the iodine content is below the label claim of 0.85%.
A&H Focal Inc. is recalling STREE OVERLORD capsules because FDA analysis found they contain sildenafil, an unapproved drug for which safety and efficacy have not been established.
Medline Industries is recalling Skin Staple Remover Kits because the iodine content is below the label claim of 0.85%.
A&H Focal Inc. is recalling LIEN CHAN FOR SEVEN DAYS capsules because they contain sildenafil, an unapproved drug with unestablished safety and efficacy.
Medline Industries is recalling Concordia Trunk Kits because the povidone-iodine prep pads contain less iodine than the label claims.
Medline Industries is recalling sterile Povidone-Iodine prep pads because the iodine content is below the labeled claim of 0.85%.
Medline Industries is recalling sterile catheter insertion kits because the iodine concentration in the prep pads is below the labeled claim.
A&H Focal Inc. is recalling Yanshijiaonang capsules because FDA analysis found they contain sildenafil, an unapproved drug for which safety and efficacy have not been established.
Medline is recalling Suture Removal Trays because the Povidone-Iodine prep pads contain less iodine than the label claims.