State
20,199 recalls have nationwide distribution and so reach Maryland. 0 additional recalls listed Maryland 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 Maryland 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.
Achieva 1.5T MR systems have incorrect warning labels on the Liquid Cooling Cabinet, missing the high voltage warning symbol. This presents a potential electrical shock risk for service personnel.
Philips Ingenia Ambition X MRI systems contain an incorrect warning label on the cooling cabinet. The label is missing high-voltage warning symbols, creating a potential electrical shock risk for service personnel.
Some Philips Intera 1.5T MRI systems have an incorrect warning label on the Liquid Cooling Cabinet that fails to properly warn service personnel of electrical shock hazards.
Glenmark Pharmaceuticals is recalling Fluocinolone Acetonide Oil 0.01% ear drops due to failed excipient specifications. The affected lots nationwide do not meet required quality standards for isopropyl alcohol content.
Sun Pharmaceutical is recalling approximately 1220 bottles of Zolpidem Tartrate Extended-Release 6.25 mg tablets distributed nationwide due to microbial contamination detected in manufacturing equipment.
Pacific Cycle is recalling about 1,700 Ascend Cabrillo and Minaret electric bikes because the battery charging wiring harness may overheat and catch fire while charging. The company has received three fire reports, including one causing second-degree burns.
Clark Associates is recalling about 53,800 Allegro plastic side chairs because the chairs can break apart while in use, creating a fall hazard. The company has received 16 reports of chairs breaking apart, resulting in two injuries.
BRS Fuel Bottles sold on Amazon from December 2020 through October 2023 do not have child-resistant closures as required by law, posing a risk of burn and poisoning to children. Consumers should stop using them immediately and contact the distributor for return or disposal.
About 12,440 Yaomiao children's tiaras with rhinestones sold on Amazon.com contain lead levels that exceed federal limits. Lead is toxic if ingested by young children and can cause adverse health effects.
Visual Comfort & Co. is recalling Maverick Coastal 60-inch outdoor ceiling fans because the blades can crack or break and fall, posing an impact injury hazard. The manufacturer has received nine reports of blade failure but no injuries or property damage so far.
Procter & Gamble is recalling Secret Dry Spray Antiperspirant due to benzene contamination in specific lot numbers. The FDA has classified this as a Class I recall.
Maquet Cardiovascular is recalling Express chest drain units with defective sterile water syringes. If not kept upright, patients risk exposure to infectious material that may cause infection, abscess, sepsis, or death.
Old Spice Sweat Defense Ultimate Captain anti-perspirant spray is being recalled due to benzene contamination. The FDA Class I recall affects products distributed nationwide and internationally.
Old Spice PURE SPORT Anti-Perspirant Spray is recalled for benzene contamination in certain lot numbers. The product was distributed nationwide and internationally.
Mead Johnson is recalling Enfamil Nutramigen Hypoallergenic Infant Formula Powder due to potential Cronobacter sakazakii contamination. Approximately 1.4 million cans with specific UPC codes (300871239418 or 300871239456) and January 1, 2025 use-by date are affected.
The FDA is recalling Secret Dry Spray antiperspirant (Lot #12001458SF) due to benzene contamination. Consumers should stop using the product immediately.
The FDA has recalled Secret Dry Spray Antiperspirant due to benzene contamination in certain lots. Affected products were distributed nationwide in the USA, Puerto Rico, Canada, and internationally.
Maquet Cardiovascular is recalling Express chest drains pre-packaged with recalled sterile water syringes. If not kept upright, patients may be exposed to infectious material, risking infection, abscess, sepsis, and death.
The Procter & Gamble Company is recalling Secret antiperspirant/deodorant spray due to the presence of benzene, a chemical contaminant. The recall affects multiple lot numbers distributed nationwide and internationally.
Old Spice Sweat Defense Pure Sport Plus anti-perspirant spray is being recalled nationwide due to benzene contamination in specific lot numbers. Consumers should discontinue use of affected products immediately.
Americaine benzocaine 20% topical anesthetic spray is being recalled nationwide due to benzene chemical contamination. The recall affects 34,704 cans with lot number 1A16420 and expiration date 01/31/2025.
Pfizer is recalling 34,000 cartons of 4.2% Sodium Bicarbonate Injection nationwide due to glass particles in the solution. Patients should immediately stop use and contact their supplier.
Pfizer Inc. is recalling Atropine Sulfate Injection due to glass particulate matter contamination in lot GY2496. This FDA Class I recall affects 24,400 cartons distributed nationwide in the USA and Puerto Rico.
Pfizer Inc. is recalling 21,200 cartons of Sodium Bicarbonate Injection (lot HA7295, expiring March 1, 2025) nationwide due to glass particle contamination. The product is distributed in the United States and Puerto Rico.
Getinge Usa Sales Inc is recalling Maquet PowerLEDII OR light systems due to a potential for the light to fall in the operating room. No injuries have been reported.