State
20,190 recalls have nationwide distribution and so reach Louisiana. 0 additional recalls listed Louisiana specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Louisiana consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
Clark Associates is recalling about 27,140 Lancaster Table & Seating Standard Height Plastic Restaurant High Chairs because the T-bar at the front can become loose, fall, or break off during use, posing a fall hazard to children.
Stiger Inc. is recalling about 3,045 Besrey Twins Strollers sold on Amazon due to entrapment, fall, and choking hazards that violate federal stroller safety regulations. Consumers should stop using the product immediately.
Victor Electric Folding Soft Bullet Toy Guns sold on Temu.com lack required blaze orange tips and have projectiles that fail to meet federal safety standards for toy weapons. The recalled toy guns pose an eye injury hazard to children.
Kawasaki is recalling approximately 19,100 units of the 2024 Mule PRO 1000 utility vehicles due to improper combustion during engine start that can pose a fire hazard. Three fires have been reported with no injuries.
Grand Rapids Chair Company is recalling approximately 5,670 wood dining chairs that can shift, break, or collapse, posing a fall hazard. The company has received three reports of the chair breaking, though no injuries have been reported.
Torquay eTrading is recalling Essential Values Golf Grip Solvent and Golf Grip Kits because they are falsely labeled as "Safe and Non-Toxic" and lack required warnings for petroleum distillates, creating a poisoning risk.
StellaLife VEGA Oral Care spray bottles have been recalled due to contamination with multiple Bacillus species organisms. The FDA Class I recall affects 31,811 bottles distributed nationwide to physician offices.
Baxter Healthcare is recalling 350 units of the Volara System Blue Ventilator Adapter Module because the handset plug may disconnect from the nebulizer port, disrupting ventilator gas flow. Affected units were distributed nationwide and internationally.
Glenmark Pharmaceuticals is recalling Potassium Chloride Extended-Release Capsules (750 mg) nationwide due to failed dissolution specifications that may affect medication delivery. Approximately 36,630 bottles are affected.
Baxter's Volara System SPU circuit kits may have a faulty handset plug that disconnects from the nebulizer adapter, preventing proper ventilator gas flow.
Glenmark Pharmaceuticals is recalling potassium chloride extended-release capsules (750 mg) nationwide due to failed dissolution specifications. Affected patients should contact their healthcare provider before making any changes to their medication.
Snapchill, LLC is recalling Knowledge Perk 'The Ace' Coffee Shandy 12 oz cans due to potential under-processing during manufacturing. The recall affects 549,146 cans distributed nationwide in the US and Canada with expiration dates from June 16, 2024 through April 16, 2025.
B. Braun Medical recalls Infusomat UNIV. 15 DROP PUMP SET due to backcheck valve malfunction that could cause medication backflow and loss of medication, resulting in adverse drug reactions.
B. Braun's Infusomat pump sets may have faulty backcheck valves causing medication to backflow between IV bags, risking reduced medication delivery and adverse reactions. All units distributed worldwide after August 2023 are affected.
B. Braun Medical is recalling 32,752 units of the Infusomat UNIV. 15 DR pump tubing set due to potential backcheck valve malfunction that could cause medication backflow between IV containers and medication loss.
Surgical image guidance software in NGENUITY 3D systems may miscalculate lens axis placement during eye rotation, potentially causing astigmatic error and decreased visual acuity.
Snapchill, LLC is recalling approximately 549,146 cans of Coffee Hound and Helm brand maple latte beverages due to potential under-processing during manufacturing.
Abbott is recalling 21,843 Proclaim DRG implantable pulse generators because the duration between the device's elective replacement indicator and end of service may be shorter than stated in product labeling.
B. Braun's Infusomat 60 IV infusion pump set is being recalled due to a backcheck valve that may malfunction, allowing medication to flow backward between IV containers and preventing proper priming of the line.
B. Braun Medical is recalling the OUTLOOK PUMP SET 3 IV infusion sets due to a potential backcheck valve malfunction that could cause medication to backflow from secondary containers into primary containers, risking adverse drug reactions and medication loss.
Snapchill, LLC recalls Mad Priest Coffee Fallen Angel with Vanilla canned beverages due to potential under-processing. Approximately 549,146 cans with expiration dates between June 16, 2024 and April 16, 2025 are affected.
Boston Scientific recalls the Autotome RX Cannulating Sphincterotome due to foreign material on the cutting wire that may prevent proper device function and extend procedure time. No injuries reported.
Abbott Proclaim XR 7 implantable pulse generators may have a shorter service life than indicated in product labeling. Approximately 9,006 units distributed worldwide are affected.
Infusomat SPACE IV infusion sets are recalled due to a backcheck valve defect that may cause medication to flow backward into primary IV bags, potentially resulting in medication loss or adverse drug reactions.
Ethicon is recalling SURGICEL FIBRILLAR hemostatic pads due to torn foil pouches that compromise the sterile barrier, traced to a specific packaging machine defect.