State
73,738 recalls have nationwide distribution and so reach Oklahoma. 5,822 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,822 recalls naming Oklahoma we have scored against our rubric, 1,040 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,493 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,822 recalls whose distribution notice names Oklahoma specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Zimmer GmbH is recalling specific cannulated orthopedic drills because an investigation found they may have been manufactured from a different material than specified.
Zimmer GmbH is recalling specific cannulated drills because an investigation found they may have been manufactured from a different material than specified.
Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the specifications.
Remel Inc is recalling 8,615 units of Thio Med w/Dex, Hem, Vit K media due to potential performance failures starting 57 days after manufacturing.
Polymer Technology Systems is recalling certain Lipid Panel test strips because they may not fit tightly into the optical block, potentially causing incorrect test results.
Remel Inc is recalling Thio Med w/Dex, Hem, Vit K media because it may fail performance testing after 57 days. The expiration date is shortened to 56 days.
Zimmer GmbH is recalling specific cannulated orthopedic screws because they may have been manufactured from a material different from the specifications.
Mallinckrodt Pharmaceuticals is recalling Amitiza (lubiprostone) capsules because 8 mcg and 24 mcg bottles were found with incorrect contents.
KaVo Dental Technologies is recalling 211 DEXIS Titanium Intraoral Sensors because incorrectly programmed calibration files may reduce image quality.
Zimmer GmbH is recalling specific cannulated orthopedic screws because an investigation found they may have been manufactured from a different material than specified.
Remel Inc is recalling 1,069 units of Thio Med w/Dex, Hem, Vit K media due to potential performance failures after 106 days.
Cook Inc. is recalling Kwart RetroInject and Salle Intraoperative Pyeloplasty Stent Sets because the instructions for use did not include a warning for stent knotting.
Zimmer GmbH is recalling V-TEK IVP step drills because they may have been manufactured from a material different from the applicable specifications.
Remel Inc is recalling Thio Med w/Dex, Hem, Vit, K media because it may fail performance testing after 57 days. The expiration date is shortened to 56 days.
Zimmer GmbH is recalling specific AO drills because they may be made from the wrong material. The products were distributed to 38 US states.
Zimmer GmbH is recalling specific AO drills because they may have been manufactured from a different material than specified.
Zimmer GmbH is recalling Drill Sys2.7 surgical instruments because they may have been manufactured from a material different from the defined specifications.
Remel Inc is recalling Thio Med w/o Ind, w/Dex media because it may fail performance testing after 106 days. The expiration date is being shortened to 105 days.
Neusoft Medical Systems is recalling six NeuViz 128 CT scanners due to a software defect that may cause image loss during specific scans.
Neusoft Medical Systems is recalling 37 NeuViz 64 CT scanners due to a software defect that can cause image loss during specific scans.
Remel Inc is recalling Thio Med culture media due to potential performance failures after 106 days. The expiration date is shortened to 105 days.
Zimmer GmbH is recalling specific 2.7mm orthopedic drills because they may have been manufactured from a material different from the specifications.
Zimmer GmbH is recalling CBS micro, countersink, cannulated, AO screws (Item Number 503004541) because they may have been manufactured from a different material than specified.
Collagen Matrix, Inc. is recalling Neomem Resorbable Collagen Membranes because they were packaged in the wrong box, potentially inside a Neomem FLEXPLUS box.
Richwell Group is recalling 160,020 pounds of frozen fish products imported from Vietnam without proper inspection. No illnesses have been reported.