State
73,827 recalls have nationwide distribution and so reach Oklahoma. 5,823 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,823 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 1,494 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,823 recalls whose distribution notice names Oklahoma specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Life Science Pharmacy Inc. is recalling Human Chorionic Gonadotropin (HCG) sublingual drops due to potential penicillin cross-contamination. The recall covers all lots distributed nationwide.
Philips Medical Systems is recalling five Allura BiPlane X-ray systems because the monitor ceiling suspension system may fall.
Quest Medical, Inc. is recalling specific MPS Delivery Sets used with cardiopulmonary bypass equipment due to intermittent seal failures during use.
Life Science Pharmacy Inc. is recalling TRI-EST Gels because they may be contaminated with penicillin.
Stryker is recalling 19,876 I.V. poles because a nonconforming latch housing may cause them to retract unexpectedly while holding medical equipment.
Western Drug is recalling Procaine HCl Injection 1% and 2% because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Basler Electric is recalling about 11,900 Class 2 electric transformers because a circuit breaker may fail to trip, posing fire and electrical shock risks.
Geritrex Corporation is recalling Polyethylene Glycol 3350-GRX Powder 100% jars because the FDA determined they are unapproved new drugs and misbranded.
Stryker is recalling 2,577 Duracon Tibial Wedge implants because they punctured the packaging's Tyvek lids, potentially compromising sterility.
Merz North America is recalling 1,616 units of Radiesse (+) Lidocaine Injectable Implant because the expiration date on the packaging is incorrect.
Merz North America is recalling Prolaryn Injectable Implant 1.0 cc Gel because the expiration date on the label is incorrect.
Geritrex Corporation is recalling Carbo-O-Philic 40 Cream tubes because the FDA determined the product is an unapproved new drug and misbranded.
Nephron Pharmaceuticals is recalling 32,490 cartons of Asthmanefrin Racepinephrine Inhalation Solution due to discoloration. The FDA classifies this as a Class II recall.
Ormco is recalling Copper NiTi Preformed Archwires because the transformation temperature listed on the label is incorrect.
Merz North America is recalling Prolaryn Plus Injectable Implants because the expiration date on the labels is incorrect. The recall covers 9,439 units distributed in the US and South Africa.
Geritrex Corp is recalling Carbo-O-Philic 40 Gel because the FDA determined it is an unapproved new drug and misbranded.
Nephron Pharmaceuticals is voluntarily recalling Asthmanefrin inhalation solution starter kits due to discoloration. The recall covers 47,754 cartons distributed nationwide.
Northwind Pharmaceuticals is recalling 40 bottles of Prednisone 20 mg tablets because the NDC number on the container is incorrect.
Kubota is recalling approximately 11,500 RTV-X1100C utility vehicles because combustible debris can contact the exhaust manifold and ignite, posing a fire hazard.
Volkswagen Group of America is recalling 2012-2013 Audi A6 and A7 vehicles because the passenger air bag system may fail to deploy in a crash.
Limoss is recalling about 2,500 lithium ion battery power packs for power recliners and lift chairs because they can overheat and pose a fire hazard.
Strick Trailers is recalling 2007, 2009, and 2015 Dry Freight Van Trailers because rear impact guard gussets increase injury risk in crashes.
Technical Consumer Products is recalling specific 14-watt LED PAR38 lamps sold at Walmart and electrical distributors due to a risk of electric shock in wet locations.
Jofran is recalling about 300 Boulder Ridge dining tables because stress fractures in the cement tops can cause the table to break. No injuries have been reported.
Volkswagen is recalling 904 2015 Audi A3 Cabriolets because incorrectly stitched seat covers may prevent side air bags from deploying properly in a crash.