State
72,913 recalls have nationwide distribution and so reach Louisiana. 6,922 additional recalls listed Louisiana specifically in their distribution scope.
Of the 6,922 recalls naming Louisiana we have scored against our rubric, 1,094 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,483 (21%) are Severe.
Which agencies issued them
These figures cover only the 6,922 recalls whose distribution notice names Louisiana specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Blackstone Parmesan Ranch Seasoning in 7.3 oz containers is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination.
Medtronic is recalling certain lots of its DLP Retrograde Cannula (Model 94725), a cardiopulmonary bypass catheter, because the sterile barrier may be breached, potentially allowing contamination. The cannulas were distributed worldwide.
UCB Biosciences is recalling CIMZIA (certolizumab pegol) prefilled syringes nationwide because of a lack of assurance of sterility. Affected lots are distributed across the US.
Fisher Tex Mex Trail Mix in 30 oz plastic jars is being recalled over the potential presence of Salmonella. 606 cases are affected.
Medtronic Perfusion Systems is recalling certain lots of the DLP Retrograde Cannula (Model 94215T) due to a potential sterile barrier breach. The affected product is a cardiopulmonary bypass vascular catheter distributed worldwide.
PS Seasoning & Spices Non Fat Dry Milk in 1 lb packs is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination.
PS Seasoning 1P Jalapeno Heat Unit is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination. 3,744 lbs are affected.
Good & Gather Mexican Street Corn Trail Mix in 8 oz bags is being recalled over the potential presence of Salmonella. 272 cases are affected.
PS Seasoning PSW21585 Save A Lot Bind 50# is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination. 992.5 lbs are affected.
Ember is recalling 2026-2027 Touring Edition trailers because incorrectly tightened shock bolts may detach, creating a road hazard and increasing crash risk.
PS Seasoning 1P Original Smokehouse Unit is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination. 5,375.6 lbs are affected.
Becton, Dickinson and Company is recalling multiple models of Swan-Ganz Catheters due to potential leaking or breaking of the proximal injectate lumen hub that could lead to infection, medication loss, or blood loss.
Zydus Pharmaceuticals is recalling Erythromycin Tablets, 250 mg, nationwide because certain lots contain N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit due to CGMP deviations.
Squirrel Brand Travelers Mix in 16 oz cans is being recalled over the potential presence of Salmonella. 3,858 cases are affected.
VitaminAlly FulviLife Complex oral liquid is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.
Medtronic is recalling certain lots of its DLP Retrograde Cannula (Model 94915), a cardiopulmonary bypass vascular catheter, due to potential sterile barrier breach.
Medtronic is recalling certain lots of DLP Retrograde Cannula (Model 94913L), a cardiopulmonary bypass catheter, due to potential sterile barrier breaches. The affected device was distributed worldwide.
Medtronic Perfusion Systems is recalling certain lots of the DLP Retrograde Cannula (Model 94913), a cardiopulmonary bypass vascular catheter, due to a potential sterile barrier breach.
Becton, Dickinson and Company is recalling Swan-Ganz Jr Catheters (models SGPT54, SGPT64P, SGPT755P) because the blue proximal injectate lumen hub may leak or break due to manufacturing changes, risking infection, medication loss, and blood loss.
Tangent Endoscopy is recalling its Tangent Single Use Digital Catheter (models TNG4002-IND and TNG-4007-6pk) due to fractures observed at the distal shaft tip without complete detachment, posing a risk during endoscopic procedures.
Becton, Dickinson and Company is recalling Swan-Ganz Pacing Catheter Model D200F7 due to a manufacturing defect that may cause the proximal injectate lumen hub to leak or break, potentially leading to infection, medication loss, or blood loss.
Medtronic is recalling certain lots of GUNDRY Retrograde Cannula (Model 94113T), a cardiopulmonary bypass catheter, due to potential sterile barrier breach in the product.
Philips Azurion X-ray imaging systems may experience impaired table movement due to mechanical wear in the Float Tabletop control. The control module defect could affect longitudinal and transverse table positioning during medical procedures.
Medtronic Perfusion Systems is recalling certain lots of the DLP Retrograde Cannula Model 94665 due to potential sterile barrier breach. The product is used in cardiopulmonary bypass procedures worldwide.
VitaminAlly Liposomal Collagen Booster is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.