State
20,072 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.
Arsell is recalling Benadryl Liquid Elixir 100 mL bottles sold on Amazon because the packaging is not child-resistant as required by federal law. The medication could poison children if ingested.
GIKPAL 10 Drawer Dressers sold on Walmart.com are recalled for tip-over and entrapment hazards to children if not anchored to a wall. About 28,590 units were sold between September 2023 and January 2025.
Weight plates on FitRx SmartBell XL dumbbells can dislodge during use, causing impact injuries. More than 60 incidents reported, linked to 7 documented injuries including bruises and contusions.
VC Group recalls 89,500 MagSafe wireless power banks because lithium-ion batteries can overheat and ignite. The company received 19 fire reports resulting in 10 minor injuries.
Kimpex ski kits for snowmobiles can detach from the vehicle, posing a crash hazard and risk of serious injury. No injuries have been reported to date.
Reckitt is recalling approximately 16,200 bottles of Woolite Delicates detergent sold exclusively on Amazon due to potential Pseudomonas bacteria contamination. The bacteria poses a serious infection risk to people with weakened immune systems or external medical devices.
Portex Endotracheal Tubes from Smiths Medical ASD, Inc. may have a smaller diameter than expected, potentially causing inadequate ventilation and patient hypoxia.
The FDA is recalling phenylephrine injection solution due to particulate matter contamination. Three lot numbers distributed nationwide are affected.
ICU Medical recalls Potassium Chloride 20 mEq IV injection due to mislabeled overwrap showing 10 mEq instead of the correct strength. The correct dose is printed on the actual container.
CareFusion 213, LLC is recalling ChloraPrep One-Step, a preoperative skin preparation drug, due to non-sterility from a package lidding breach allowing fungal contamination. The recall affects 205,440 applicators distributed nationwide and in Canada.
ICU Medical recalls Potassium Chloride Injection (lot 1023172) whose overwrap labeled as 10 mEq may contain 20 mEq containers, creating overdose risk. Product distributed nationwide.
Medtronic is recalling 316,205 aortic root cannulas due to unexpected loose material in the male luer connector. If not identified before use, this defect could cause stroke; if identified, it may delay surgery.
ZOLL is recalling 8,744 Powerheart G5 AED units that may fail their self-test if exposed to extreme temperatures or humidity, potentially masking device malfunctions.
Spectrum Medical is recalling Quantum Perfusion blood pumps due to potential fluid leakage during priming or clinical use. The issue affects approximately 1,487 units distributed nationwide.
Aesculap Inc is recalling 917,965 units of nonsterile hemostatic forceps across multiple models because the clamps can break when used beyond design specifications. No injuries have been reported.
Breckenridge Pharmaceutical recalls 11,100 bottles of Duloxetine 60mg capsules distributed nationwide due to the presence of N-nitroso-duloxetine impurity exceeding FDA recommended interim limits from manufacturing deviations.
Trader Joe's branded Solid White Albacore Tuna is being recalled because the easy-pull lids were not properly secured, potentially allowing Clostridium botulinum contamination. Approximately 14,147 cases were distributed nationwide.
H-E-B branded Solid White Albacore Tuna is being recalled because its easy-pull lid may not be properly secured, risking contamination with Clostridium botulinum. The recalled products were distributed nationwide.
Beckman Coulter is recalling the DxI 9000 Access Immunoassay Analyzer due to a mechanical defect in the wash wheel mixer that may prevent the device from operating properly. The defect can cause test delays or cancellation.
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.
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.
DePuy Mitek's COR Disposable Cartilage Transplant System is being recalled because some units are missing a pin in the graft loader component, which could affect surgical function.
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.
Nephron Sterile Compounding Center is recalling Sodium Chloride Injection 9% due to potential leakage at the IV bottle port, which could compromise sterility. Affected lots were distributed nationwide.
Aesculap Inc is recalling 19,979 hemostatic forceps across 18 models because clamps can break when instruments are used outside of design specifications.