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All product recalls affecting District of Columbia.
Includes nationwide recalls (tagged “Nationwide”) and recalls with District of Columbia in the distribution area.
This recall involves seven styles of Marie-Chantal children's 100% organic cotton or 100% pima cotton nightgowns, three styles of children's pajama sets and two bathrobe styles. The nightgowns were sold in white with a bird print, white with a feather print, white with a bunny print, white with multicolor dots, pink or pink and white with a star and crown print, white with a pink flower print, and pink with a kitten and tea pot print. The children's two-piece pajamas were sold in pink with a kitten and tea pot print two-piece pajama set, golden crest two-piece pajama set, and pink or cream with an angel wing print. The robes were sold in white and pink or white and blue color combinations with a star and crown print, and plain white. The nightgowns and pajama sets were sold in children's sizes 2 years through 10 years, and the robes were sold in sizes small, medium and large. "Marie-Chantal" and the RN number 103490 are printed on a sewn-in seam label.
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Jayco, Inc. (Jayco) is recalling certain 2024 Entegra Condor, Jayco Granite Ridge, 2025 Jayco Alante SE, Redhawk SE, and Entegra Odyssey SE motorhomes. The Occupant and Cargo Carrying Capacity (OCCC) on the Federal label may be incorrect and allow the vehicle to be overloaded. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 120, "Wheels and Rims - other than passenger cars."
The battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.
Shyft Group (Shyft) is recalling certain 2024-2025 Blue Arc BA4L-800 vehicles. The headlight horizontal adjustment stud is missing a cover, allowing for horizontal adjustment of the headlight beam. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment."
Airstream, Inc. (Airstream) is recalling certain 2021-2025 Airstream Classic 33', 2024-2025 Classic 30', and 2025 Classic 28' travel trailers. The sofa footrest switch may have underrated wiring, which can allow the wiring to overheat.
Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
Daimler Coaches North America (Daimler Coaches) is recalling certain 2022-2025 Mercedes Benz Tourrider Business and Premium transits buses. The fixate stop bracket on the driver's seat backrest may not be installed. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 207, "Seating Systems," and 210, "Seat Belt Assembly Anchorages."
Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended interim limit.
Presence of foreign substance: Presence of Benzene.
Failed Dissolution Specifications
Presence of foreign substance: Presence of Benzene.
Sumitomo Rubber Industries, Ltd. (Sumitomo) is recalling certain Dunlop GPR-300F tires, size 110/70R17M/C 54H. The tires may have a defect that causes inner liner bulging and looseness at the tire breaker edge. As such, these tires fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 119, "New Pneumatic Tires- Other than Passenger Cars."
Chemical Contamination: This recall has been initiated due to detected trace levels of benzene.
cGMP Deviations: The recall was initiated due to detected trace levels of benzene in a specific lot of this product lot (MYX46W), however out of an abundance of caution, the firm voluntarily recalled all La Roche-Posay Effaclar Duo Dual Action Acne Treatment lots.
cGMP Deviations: The recall was initiated due to detected trace levels of benzene in a specific lot of this product lot (MYX46W), however out of an abundance of caution, the firm voluntarily recalled all La Roche-Posay Effaclar Duo Dual Action Acne Treatment lots.