State
72,940 recalls have nationwide distribution and so reach Iowa. 5,581 additional recalls listed Iowa specifically in their distribution scope.
Of the 5,581 recalls naming Iowa we have scored against our rubric, 909 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,317 (24%) are Severe.
Which agencies issued them
These figures cover only the 5,581 recalls whose distribution notice names Iowa specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Zydus Pharmaceuticals is recalling 36,624 bottles of Bromocriptine Mesylate Capsules USP 5 mg after an out of specification result for the 2-Bromoergine impurity.
ASP Global is recalling 49,000 SAFE-T-FILL micro capillary blood collection tubes, 200 microlitres with lithium heparin and plasma separator gel, over an inadequate quality system.
ASP Global is recalling 64,850 SAFE-T-FILL micro capillary blood collection tubes, 300 microlitres with clot activator and serum separator gel, over an inadequate quality system.
Medtronic is recalling 3,850 HR-ACT clotting time cartridges after trace amounts of dry blood were observed on the external carton label and instructions in five boxes.
ASP Global is recalling 77,500 SAFE-T-FILL plastic blood gas capillary tubes, 150 microlitres untreated, over an inadequate quality system.
DermaRite Industries is recalling 2,389 bottles of DermaSarra external analgesic because it was made at the same facility where other products and lots were found to be contaminated.
DermaRite Industries is recalling 381,619 units of PeriGuard Ointment because it was made at the same facility where other products and lots were found to be contaminated.
DermaRite Industries is recalling 115,994 containers of GelRite Instant Hand Sanitizer because it was made at the same facility where other products were found contaminated.
DermaRite Industries is recalling 15,465 cartridges of San-E-Foam alcohol hand sanitiser because it was made at the same facility where other products were found contaminated.
ASP Global is recalling 620,502 SAFE-T-FILL end caps for blood gas capillaries over an inadequate quality system with unvalidated manufacturing processes.
DermaRite Industries is recalling 16,006 units of PeriGiene health care antiseptic because it was made at the same facility where other products were found contaminated.
DermaRite Industries is recalling 5,876 units of McKesson Skin Protectant with lanolin because it was made at the same facility where other products were found contaminated.
ASP Global is recalling 1,500 SAFE-T-FILL micro capillary blood collection tubes, 200 microlitres with clot activator in an amber microtube, over an inadequate quality system.
ASP Global is recalling 947,100 SAFE-T-FILL plastic blood gas capillary tubes, 150 microlitres with sodium heparin, over an inadequate quality system.
ASP Global is recalling 6,600 SAFE-T-FILL micro capillary blood collection tubes, 300 microlitres with clot activator, over an inadequate quality system.
DermaRite Industries is recalling 7,736 tubes of DermaKleen antiseptic lotion soap because it was made at the same facility where other products were found contaminated.
DermaRite Industries is recalling 3,178 bottles of 4-N-1 Skin Protectant No Rinse Wash Cream because it was made at the same facility where other products were found contaminated.
ASP Global is recalling 2,100 SAFE-T-FILL micro capillary blood collection tubes, 200 microlitres with sodium fluoride, over an inadequate quality system.
ASP Global is recalling 121,750 SAFE-T-FILL plastic blood gas capillary tubes, 115 microlitres, over an inadequate quality system with unvalidated processes.
DermaRite Industries is recalling 37,272 tubes of Renew PeriProtect because it was made at the same facility where other products and lots were found to be contaminated.
DermaRite Industries is recalling 1,480 packets of DermaFungal antifungal cream because it was made at the same facility where other products and lots were found contaminated.
ASP Global is recalling 160,250 SAFE-T-FILL plastic blood gas capillary tubes, 230 microlitres with sodium heparin, over an inadequate quality system.
Golden State Medical Supply is recalling 24,869 bottles of Niacin Extended-Release Tablets USP 1,000 mg for failed dissolution specifications.
ASP Global is recalling 1,000 SAFE-T-FILL plastic blood gas capillary tubes, 115 microlitres with sodium heparin, over an inadequate quality system.
DermaRite Industries is recalling 2,673 tubes of DermaMed Ointment because it was made at the same facility where other products and lots were found to be contaminated.