State
72,940 recalls have nationwide distribution and so reach Kansas. 5,723 additional recalls listed Kansas specifically in their distribution scope.
Of the 5,723 recalls naming Kansas we have scored against our rubric, 1,045 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,228 (21%) are Severe.
Which agencies issued them
These figures cover only the 5,723 recalls whose distribution notice names Kansas specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
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.
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.
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.
Teva Pharmaceuticals is recalling six lots of Metoprolol Succinate Extended-Release Tablets 100 mg after the product failed dissolution specifications.
Mack Trucks is recalling 2022-2027 TerraPro trucks because engine software may allow starting while in gear, increasing crash risk.
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.
Acme United Corporation is recalling Med-Nap Cleansing Towelettes in bulk cases over current good manufacturing practice deviations.
HTO Nevada, trading as Kirkman, is recalling one lot of Maximum Zone 1 4% Lidocaine Cream because the stability data does not support the labeled expiry date.
Acme United Corporation is recalling Dynarex BZK Antiseptic Towelettes in 1,000-packet bulk packs over current good manufacturing practice deviations.
Acme United Corporation is recalling Green Guard Antiseptic Wipes over current good manufacturing practice deviations.
The Harvard Drug Group is recalling one lot of Midodrine Hydrochloride Tablets 5 mg because of a defective container with inadequately sealed blister packaging.
Acme United Corporation is recalling Antimicrobial Alcohol Hand Wipes containing 70% isopropyl alcohol over current good manufacturing practice deviations.
Acme United Corporation is recalling Medi-First Antiseptic Wipes over current good manufacturing practice deviations.
Acme United Corporation is recalling Dynarex BZK Antiseptic Towelettes in 100-packet cartons over current good manufacturing practice deviations.
Acme United Corporation is recalling Med-Nap BZK Antiseptic Towelettes in bulk packs 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.
HTO Nevada, trading as Kirkman, is recalling Five-Star Vasocaine Spray because the stability data does not support the labeled expiry date.
Acme United Corporation is recalling Wipes Plus Hand Sanitizing Alcohol Free BZK Wipes over current good manufacturing practice deviations.
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.
Harbin Jixianglong Biotech is recalling a further lot of Semaglutide for prescription compounding because process validation and bacterial endotoxin method validation were not completed before distribution.
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.
Harbin Jixianglong Biotech is recalling Semaglutide for prescription compounding use because process validation and bacterial endotoxin method validation were not completed before distribution.
Acme United Corporation is recalling Med-Nap Cleansing Towelettes over current good manufacturing practice deviations.