State
72,936 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 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Volvo is recalling certain 2025-2026 EX30 and 2026 EX30CC vehicles because the seat belt warning system may not activate the audible warning chime. This fails FMVSS 208.
Volkswagen is recalling certain 2025–2026 Jetta vehicles because the transmission ground wire may not have been properly connected during assembly, creating an open electrical circuit that could increase fire risk.
Diagnostica Stago is recalling four lots of the STA Liatest Free Protein S kit because of the potential for out-of-range results and underestimation of free protein S in normal patient plasmas.
Mylan Pharmaceuticals is recalling two lots of Amnesteem (Isotretinoin) Capsules 40 mg after the product failed dissolution specifications.
Aesculap is recalling MINOP Trocar 150 mm with 6.0 mm working channel, model FF399R, because of the potential for the trocar shaft to be too long.
Siemens Healthcare Diagnostics is recalling all lots of the Atellica CH Urine Albumin assay because falsely depressed patient results may occur above the measuring interval.
Olympus is recalling ShockPulse-SE Lithotripsy System single use probes after further instances of the generator remaining in a blinking phase waiting to recognize the transducer.
Olympus is recalling all lots of its Single Use Biopsy Valve, model MAJ-1218, because of the potential for rubber fragment detachment during use.
Teva Pharmaceuticals is recalling six lots of Metoprolol Succinate Extended-Release Tablets 100 mg after the product failed dissolution specifications.
B. Braun Medical is recalling 21GA Winged Infusion single packs, model 7A3842, because the needle tip may be dull or blunt, difficult to advance, or may break.
B. Braun Medical is recalling 21G x 4.4 cm Winged Infusion devices, model 7B3050, because the needle tip may be dull or blunt, difficult to advance, or may break.
Teva Pharmaceuticals is recalling six lots of Metoprolol Succinate Extended-Release Tablets 50 mg after the product failed dissolution specifications.
Teva Pharmaceuticals is recalling six lots of Metoprolol Succinate Extended-Release Tablets 25 mg after the product failed dissolution specifications.
Olympus is recalling the ShockPulse-SE Lithotripsy System Generator after further instances of the generator remaining in a blinking phase waiting to recognize the transducer.
Olympus is recalling all lots of its Single Use Biopsy Valve, model MAJ-210, because of the potential for rubber fragment detachment during use.
Roche is recalling cobas pro sample supply units on software versions before 03-02 because a defect can make the analyzer repeat the last calculated result for all later measurements.
Olympus is recalling ShockPulse-SE Lithotripsy System reusable probes after further instances of the generator remaining in a blinking phase waiting to recognize the transducer.
ARBOC is recalling 2018-2026 Spirit of Freedom and Spirit of Mobility buses because incorrectly installed rear brake lines may cause the anti-lock brake system to malfunction.
Mack Trucks is recalling 2022-2027 TerraPro trucks because engine software may allow starting while in gear, increasing crash risk.
Acme United Corporation is recalling Medi-First Antiseptic Wipes over current good manufacturing practice deviations.
Datascope is recalling the CS300 IABP running software version C.01 because the battery runtime and cycle specifications in the device's Instructions for Use need to be updated.
Acme United Corporation is recalling BZK Antiseptic Towelettes sold under the Piedmont, Touchpoint, Wellstar Cobb and FSR names over current good manufacturing practice deviations.
Acme United Corporation is recalling Children's Healthcare of Atlanta Instant Hand Sanitizing Wipes over current good manufacturing practice deviations.
Acme United Corporation is recalling First Aid Only BZK Antiseptic Towelettes over current good manufacturing practice deviations.
Acme United Corporation is recalling First Aid Only BZK Antiseptic Towelettes in bulk packs over current good manufacturing practice deviations.