State
72,936 recalls have nationwide distribution and so reach Oklahoma. 5,788 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,788 recalls naming Oklahoma we have scored against our rubric, 1,033 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,238 (21%) are Severe.
Which agencies issued them
These figures cover only the 5,788 recalls whose distribution notice names Oklahoma specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mylan Pharmaceuticals is recalling two lots of Amnesteem (Isotretinoin) Capsules 40 mg after the product failed dissolution specifications.
Olympus is recalling all lots of its Single Use Biopsy Valve, model MAJ-1218, because of the potential for rubber fragment detachment during use.
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.
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.
Teva Pharmaceuticals is recalling six lots of Metoprolol Succinate Extended-Release Tablets 25 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.
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 single use probes after further instances of the generator remaining in a blinking phase waiting to recognize the transducer.
Teva Pharmaceuticals is recalling six lots of Metoprolol Succinate Extended-Release Tablets 50 mg after the product failed dissolution specifications.
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.
Acme United Corporation is recalling WP WipesPlus Hand Sanitizing 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 Wipes Plus Hand Sanitizing Alcohol Free BZK Wipes 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.
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.
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 Med-Nap BZK Antiseptic Towelettes in bulk packs over current good manufacturing practice deviations.
Acme United Corporation is recalling First Aid Only Hand Sanitizing Wipes 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 First Aid Only BZK Antiseptic Towelettes in 100-count packs over current good manufacturing practice deviations.
Datascope is recalling the CS100 IABP running software version Q.01 because the battery runtime and cycle specifications in the device's Instructions for Use need to be updated.
Acme United Corporation is recalling Dynarex BZK Antiseptic Towelettes in 1,000-packet bulk packs over current good manufacturing practice deviations.
HTO Nevada, trading as Kirkman, is recalling one lot of Maximum Zone 2 4% Lidocaine Cream because the stability data does not support the labeled expiry date.
HTO Nevada, trading as Kirkman, is recalling Five-Star Vasocaine Spray because the stability data does not support the labeled expiry date.