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All product recalls affecting Montana.
Includes nationwide recalls (tagged “Nationwide”) and recalls with Montana in the distribution area.
This recall involves Specialized Vado and Como IGH e-bikes with chain/belt guards. The recalled e-bikes have an internal gear hub (IGH) and no rear derailleur (gear shift). The Specialized Bicycle brand name is located on the bike frame and the bikes are offered in a variety of colors, including black, limestone, red, sand, sea foam, navy, purple, white, gray, raspberry, umber, dark gray and yellow. The e-bikes have the following model numbers printed on the white and black serial number label located on the underside of the bicycle's top tube. Recalled Specialized Bicycle Model Numbers COMO 3.0 IGH COMO 5.0 IGH UL VADO 3.0 IGH STEP THROUGH UL COMO 3.0 IGH UL COMO SL 4.0 VADO 3.0 IGH UL COMO 4.0 IGH COMO SL 5.0 VADO 5.0 IGH COMO 4.0 IGH UL VADO 3.0 IGH VADO 5.0 IGH ST COMO 5.0 IGH VADO 3.0 IGH ST VADO 5.0 IGH STEP THROUGH UL
This recall involves children's steel utility bunk beds sold by Interior Resources. The steel twin size bunk beds were sold in a heavy-duty powder coat finish in black or brown and have a ladder and a guardrail.
This recall involves George Oliver-branded dressers. The six-drawer, wooden double dressers measure about 31 inches tall, 47 inches wide and 15-½ inches deep, and were sold in a cream color.
This recall involves APOTHEKE's 26 oz. (761 g) Pumpkin Ginger 3-Wick Scented Candles. The 3-wick candles are white and were sold in a 26 oz. (761 g) amber glass container. "APOTHEKE" is printed in gold on the front of the container. Batch code "CB-240603" is printed on a label affixed to the underside of the container.
This recall involves NFH Dietary Supplement bottles for Iron SAP, Heme Iron SAP and Prenatal SAP. The bottles are white with the brand name "NFH" and the firm's logo of a leaf in blue. The date code is on the bottom of the bottle. The recalled dietary supplement bottles have the following description and come in various sizes: Product Name Description Sizes Date Codes Iron SAP Iron Glycinate 60 Capsules (1029U) 120 Capsules (1167U) 60 capsules 5398705/31/2027 5398805/31/2027 5398512/31/2026 5398612/31/2026 5398306/30/2026 5398406/30/2026 N00274 07/31/2025 120 capsules 538975/31/2027 539875/31/2027 539885/31/2027 5398512/31/2026 5398612/31/2026 539846/30/2026 N00274 6/30/2025 Heme Iron SAP (Porcine) Superior Absorption and Bioavailability 60 Capsules (1124U) N00265 - 03/31/2025 53809 - 05/31/2026 53810 - 07/31/2026 57807 - 10/30/2026 53811 - 10/31/2026 57806 - 10/31/2026 62379 - 08/31/2027 Prenatal SAP Multivitamin 180 Capsules (1034U) 5821709/30/2027 5822009/30/2027 5736105/31/2027 5736905/31/2027 5737005/31/2027 5737205/31/2027 5821405/31/2027 5396803/31/2027 5719401/31/2027 5736001/31/2027 5396311/30/2026 5396411/30/2026 5396511/30/2026 5396611/30/2026 5396711/30/2026 5395410/31/2026 5395610/31/2026 5395810/31/2026 5396010/31/2026 5396110/31/2026 5396210/31/2026 5395307/31/2026 5394605/31/2026 5394504/30/2026 N00287 08/31/2025 N00285 04/30/2025 N00284 03/31/2025
This recall involves LINKCOO corded window shades. The roller shades were sold in white, gray and black, and in sizes ranging between 10 and 75 inches wide and 79 inches high. "LINKCOO" is printed on the label sticker on the shades' lower pole.
Due to a potential open seal in the sterile barrier packaging.
Due to a potential open seal in the sterile barrier packaging.
Due to a potential open seal in the sterile barrier packaging.
Corp. Micro Bird, Inc. (Micro Bird) is recalling certain 2012, 2015-2019, and 2024 G5 school buses equipped with Type 2 seat belts. The seat reinforcement supports may not have been installed. As such, these vehicles fail to comply with Federal Motor Vehicle Safety Standard numbers 207, "Seating Systems" and 210, "Seat Belt Assembly Anchorages."
An issue has been identified in the production of the RTS873 robotic total stations that may result in the green aiming laser output power being above its laser safety Class 2 classification.
CGMP Deviations; detection of Nitrosamine Drug Substance-Related Impurities (NDSRI), N-nitroso-desmethyl-diphenhydramine (n-dph), above the FDA Recommended Intake Limit
CGMP Deviations: presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the recommended interim limit.
Mack Trucks, Inc. (Mack) is recalling certain 2022-2025 Mack LRBE trucks. The high voltage batteries may have loose hardware that can fall inside the battery pack and create a short circuit.
Daimler Trucks North America, LLC (DTNA) is recalling certain 2026 Freightliner eM2, Freightliner 108SD, Freightliner 114SD, Freightliner Cascadia, 2025-2026 Freightliner Business Class M2, Western Star 47X, and Western Star 49X vehicles. A software error in the advanced signal and actuator module for the automatic emergency braking system may cause the brake lights to fail to illuminate.
Lucid USA, Inc. (Lucid) is recalling certain All-Weather Floor Mats without anchors, model numbers ending in -00. Please see the recall report for a complete list of all affected part numbers. The floor mats may move and trap the accelerator pedal, causing unintended acceleration.
Volvo Trucks North America (Volvo Trucks) is recalling certain 2023-2025 VNR Electric trucks. The high voltage battery may contain loose hardware, which can create a short circuit inside the battery cells.
The hip cup liner that was packaged with the incorrect labeling. HDL-060-C22S-000101 from Lot 1788258 contained a hooded liner, but it was labeled to have a standard liner.
Keystone RV Company (Keystone) is recalling certain 2025 Kodiak 2900FKSP and 308BHSL travel trailers. The patio travel latch screws may become loose, causing the patio latch to detach during transit.
Boston Scientific has identified that IceSeedTM CX needles manufactured between April 2024 and February 2025 have been programmed with DEMO settings instead of Commercial settings (see Affected Product Listing). Upon initial connection of an IceSeed CX needle to the Cryoablation System, the user will be prompted to perform the Needle Integrity and Functionality Test (NIT) per standard protocols. The affected needles perform as intended unless they are disconnected and reconnected to any channel after testing. In this case, the Cryoablation System will prompt re-execution of the NIT.