State
20,371 recalls have nationwide distribution and so reach Maine. 0 additional recalls listed Maine 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 Maine 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.
Huffy Corporation is recalling about 28,550 Blue's Clues Foot to Floor Ride-on Toys because the toy can tip forward when young children ride it, causing falls and injuries. The company has received 19 reports of children falling forward, resulting in 18 facial injuries.
Polaris Industries is recalling about 2,300 Model Year 2022 PATRIOT BOOST RMK KHAOS and PATRIOT BOOST PRO RMK snowmobiles because the primary clutch bolt can break, causing clutch components to separate and create a projectile hazard.
About 190 Big Game Hunters Mud Kitchens are being recalled because the brass water tap contains lead levels that exceed federal safety limits. Lead is toxic if ingested by young children.
Trek is recalling Model Year 2022 Speed Concept SLR bicycles, MY 2021-2022 Emonda SLR bicycles, and MY 2020-2021-2022 Bontrager Aeolus RSL VR-C aftermarket handlebar stems because carbon handlebars can crack, posing fall and crash hazards.
Epoch Everlasting Play is recalling about 8,200 Kidoozie My First Activity Desk Toys due to entanglement and entrapment hazards. A protruding knob can become entangled with clothing, and the handle opening poses a jaw entrapment risk to children under 18 months.
Navitas steel rolling chassis for utility vehicles are recalled because the throttle pedal can stick in the depressed position, creating crash and injury hazards. About 3,700 units distributed nationwide from June 2020 through April 2022 are affected.
IKEA is recalling METALLISK Espresso Makers with stainless-steel safety valves because the units can burst and expel hot contents, causing burn and scald injuries. About 2,100 units sold in the U.S. are affected.
HeartWare HVAD System Batteries are being recalled due to electrical faults that may prevent the battery from powering the device controller, accepting charges, or maintaining charge. Approximately 19,616 batteries distributed worldwide are affected.
Wilbur's of Maine Milk Chocolate Covered Blueberries are recalled because the product contains undeclared almonds, posing a risk to consumers with almond allergies.
Trinity Sterile's Wolf Pak Premium Dressing Change Kit is mislabeled as latex-free but contains natural rubber latex in component 94-7002. This poses a risk to people with latex allergies.
Nephron Sterile Compounding Center is recalling one lot of Neostigmine Methylsulfate Injection due to potential cross-contamination from product carryover during manufacturing. The recall affects 13,500 vials distributed nationwide.
Becton Dickinson recalls 9,340 units of BD PhaSeal Y-Site Connectors (Catalog 515304) due to incorrect expiration dates printed on product labels that extend beyond the actual product expiration.
Family Dollar is recalling SKYN Original, Elite, and LS non-latex condoms due to improper storage. Products sold between May 1 and June 10, 2022 were not stored in temperature-controlled conditions.
Baxter Healthcare recalls 85,680 bags of acetaminophen injection nationwide due to temperature abuse in distribution. Product was shipped in refrigerated trucks despite being labeled for room temperature storage.
Wolf-Pak Premium Dressing Kits labeled latex-free are being recalled because a component contains natural rubber latex, posing a risk to people with latex allergies.
Crown Prince Quality Smoked Baby Clams (3 oz cans, UPC 0 73230 00853 5) are recalled due to detectable PFAS contamination. Approximately 211,716 cans distributed nationwide are affected.
Stradis Medical is recalling NARMD MEDICAL DEPOT Iris Curved Scissors (Part Number ZZ-0697) because the sterile barrier may be compromised, potentially exposing patients to contamination during surgical procedures.
Micro Therapeutics is recalling Echelon-14 Micro Catheters because outer packaging was exposed to moisture during transport. The moisture exposure could compromise the sterility or function of the device.
Nephron Pharmaceuticals is recalling Ketorolac Tromethamine Injection due to manufacturing deviations that could lead to cross-contamination. The recall affects 5,040 vials distributed nationwide.
Nephron Sterile Compounding Center is recalling 2,030 bags of injectable bupivacaine due to potential cross-contamination from manufacturing process defects. No illnesses have been reported.
Akorn, Inc. is recalling 14,712 bottles of PrednisoLONE Oral Solution (15 mg/5 mL) due to incomplete induction seals in containers. No illnesses have been reported, but the defect may affect product integrity.
Zydus Pharmaceuticals recalls Fulvestrant Injection lot B200076 due to failed purity and stability specifications. Distributed nationwide; expiration January 31, 2024.
Family Dollar is recalling Veriquick Pregnancy Test 2CT kits (SKU 903756) sold from May 1 to June 10, 2022 due to improper storage outside temperature-controlled areas.
Trinity Sterile's IV catheter dressing trays are mislabeled as latex-free despite containing natural rubber latex in component 94-7002, risking allergic reactions in latex-sensitive users.
Micro Therapeutics is recalling Echelon-14 microcatheters whose outer carton packaging was exposed to a wet substance during transport, posing a risk to device sterility.