State
19,789 recalls have nationwide distribution and so reach New Mexico. 0 additional recalls listed New Mexico 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 New Mexico 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.
Breckenridge Pharmaceutical is recalling 11,125 bottles of Duloxetine 20mg capsules nationwide due to N-nitroso-duloxetine impurity above FDA-recommended limits. The impurity was detected during quality control testing.
Genova branded Yellowfin Tuna in Extra Virgin Olive Oil is being recalled because its easy-pull lid may not be properly secured, potentially allowing clostridium botulinum contamination.
The ZOLL Powerheart G5 automated external defibrillator may fail its self-test after prolonged exposure to extreme temperatures or humidity levels. This could prevent proper device functioning in an emergency.
Trader Joe's Solid White Albacore Tuna (5 oz cans) is being recalled due to improperly secured lids that may allow contamination with Clostridium botulinum. Affected products have Best By dates of 01/08/2028 or 01/09/2028.
Trader Joe's Solid White Albacore Tuna in Water is being recalled because improperly secured easy-pull lids may allow contamination with Clostridium botulinum.
ZOLL Powerheart G5 AED devices may fail their self-test if exposed to extreme temperatures or humidity. Approximately 56,981 units are being recalled nationwide and internationally.
Aesculap is recalling 47,078 surgical forceps designed to control bleeding. The devices' clamps break when used outside design parameters, potentially compromising their effectiveness.
Genova branded Yellowfin Tuna cans are being recalled because the easy-pull lid was not properly secured, which may cause Clostridium botulinum contamination. The recall affects 14,147 cases distributed nationwide with best-by dates from December 2027 through January 2028.
Intuitive Surgical has recalled 439 Da Vinci 5 surgical console foot tray pedals due to spring failures that can cause pedals to remain pressed and interfere with normal surgical robot operation.
Chicken of the Sea recalls Genova branded solid white tuna nationwide due to improperly secured easy-pull lids that may allow Clostridium botulinum contamination.
Aesculap is recalling 1,147 hemostatic forceps due to clamp breakage risk when used beyond design specifications. Units were distributed nationwide and internationally to healthcare providers.
ZOLL is recalling certain Powerheart G5 AED units that may fail their self-test when exposed to extreme temperatures or humidity. The affected devices could fail to function properly in emergencies.
Chattem Inc. is recalling Unisom SleepMelts diphenhydramine HCl 25 mg tablets nationwide due to a nitrosamine impurity detected above FDA's acceptable daily intake limit. Affected lots expire between May 2025 and April 2026.
DePuy Mitek is recalling COR Disposable Kit cartilage transplant systems because some units lack the pin in the graft loader component. The manufacturing defect may prevent proper device function during surgical use.
Chicken of the Sea is recalling 14,147 cases of Van Camp's Solid Light Yellowfin Tuna due to improperly secured easy-pull lids that may allow Clostridium botulinum contamination. No illnesses have been reported.
CardioFocus is recalling 833 units of CardiFocus Heartlight X3 cardiac catheters due to potential damage to the sterile barrier pouch that could compromise product sterility. Affected units were distributed worldwide.
ZOLL is recalling certain Powerheart G5 automated external defibrillators (AED) due to the potential for devices to fail their self-test when exposed to extreme temperatures or humidity.
Breckenridge Pharmaceutical recalls 14,749 bottles of duloxetine 30mg delayed-release capsules due to N-nitroso impurity above FDA safety limits. Patients taking this medication should contact their healthcare provider to verify if their prescription is affected.
Kids by babyganics SPF 50 sunscreen is being recalled due to chemical contamination. Approximately 449,502 units distributed nationwide in the U.S. and Canada are affected in this FDA Class II recall.
Sublue is recalling about 40,370 Mix underwater scooters and batteries with lithium-ion cells that can overheat and catch fire. Reports include 8 fires, 1 injury, and significant property damage.
Onasti Toddler Tower Stools sold on Amazon can collapse or tip over while in use, posing fall and injury risks. Recalls follow four reports of incidents, including injuries.
Meijer is recalling about 6,050 Konwin desktop heaters because the fan can fail to turn on, causing the unit to overheat and ignite. The company received eight reports of fans burning and melting, but no injuries have been reported.
HabiLife Direct retractable safety gates (model SG021) are recalled due to an entrapment hazard where children's torsos can fit through gaps between the gate and floor. About 880 units sold on Amazon from September 2024 through January 2025.
BMC recalled about 1,300 Kaius 01 bicycles because the fork steerer tube can crack and separate during use, posing a fall hazard. No injuries reported; consumers should stop using them and contact dealers for free fork replacement.
Gerolsteiner 750ml sparkling water bottles sold at Trader Joe's locations are being recalled because the glass bottles can crack, creating a laceration hazard. No injuries have been reported.