Official product recall notices and clearly labeled enforcement reference records.
Reference notice · device
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the …
Cambridge, MA, US · Updated 9/25/2026, 12:00:00 AM UTC
Source: FDA — device enforcement referenceReference notice · device
There are identified discrepancies between the sterilization parameters listed in the Instructions for Use and the sterilization parameters listed in the Japanese package insert.
Center Valley, PA, US · Updated 9/25/2026, 12:00:00 AM UTC
Source: FDA — device enforcement referenceReference notice · device
Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gloves may lead to healthcare personnel and patient exposure to infectious pathogens leading to infection or cross-contamination, or exposure to chemical agents leading to irritation or systemic toxicities.
Grove City, OH, US · Updated 9/25/2026, 12:00:00 AM UTC
Source: FDA — device enforcement referenceReference notice · device
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the …
Cambridge, MA, US · Updated 9/25/2026, 12:00:00 AM UTC
Source: FDA — device enforcement referenceReference notice · device
hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result.
San Diego, CA, US · Updated 9/25/2026, 12:00:00 AM UTC
Source: FDA — device enforcement referenceReference notice · device
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the …
Cambridge, MA, US · Updated 9/25/2026, 12:00:00 AM UTC
Source: FDA — device enforcement referenceReference notice · consumer
This recall involves NEWDERY power banks with model number ZHX-PB22. The power banks are black with yellow cables. The brand name “NEWDERY” is engraved on the front and the model number “ZHX-PB22” is printed on the back.
US · Updated 9/24/2026, 12:00:00 AM UTC
Source: CPSC — consumer recall noticesReference notice · consumer
This recall involves Hyperfuels ethanol and methanol fuel containers. The methanol container bears the Hyperfuels logo in red and associated phone number, the label bears “Methanol”, “Methanol, 3, UN1230, II”, and “Flammable Liquid” in black lettering. The ethanol container bears “E98”, “1 US Quart”, “Hyperfuels LLC” a…
US · Updated 9/24/2026, 12:00:00 AM UTC
Source: CPSC — consumer recall noticesReference notice · consumer
This recall involves WinxMatrs-branded mattresses. The black mattresses are 10 inches thick and were sold in a twin size. They were sold compressed in a box. The size and the brand are printed on the mattress’ sewn-in labels.
US · Updated 9/24/2026, 12:00:00 AM UTC
Source: CPSC — consumer recall noticesReference notice · consumer
This recall involves 5Color-branded bicycle helmet and pads sets. The sets consist of a pink helmet, knee and elbow pads. Only the size small helmets are included in this recall. The helmets are size small (S), fitting a head circumference of about 18 to 22 inches, and have black padding, black straps, a black and a bl…
US · Updated 9/24/2026, 12:00:00 AM UTC
Source: CPSC — consumer recall noticesReference notice · consumer
This recall involves The Blue Cactus Company Reclining Chair 2500 mAh battery packs with model number RWX-RBP02. The battery packs are black with the brand logo and brand name of “The Blue Cactus Company” imprinted on the front. The recalled battery packs can be identified by the model number RWX-RBP02 printed on the r…
US · Updated 9/24/2026, 12:00:00 AM UTC
Source: CPSC — consumer recall noticesReference notice · device
There is an error in the product description on the Unique Device Identification (UDI) label. These discrepancies in labeling do not align with the approved product or product specifications and may lead to incorrect product identification or selection, potentially resulting in use with an incompatible bed frame.
Deerfield, IL, US · Updated 9/24/2026, 12:00:00 AM UTC
Source: FDA — device enforcement referenceReference notice · consumer
This recall involves smart glasses with model number AIR3 and are used for AI translation, AI-assisted productivity and media streaming. The recalled products are black with “AIR3” and “INMO” printed on a label on the right temple of the product.
US · Updated 9/24/2026, 12:00:00 AM UTC
Source: CPSC — consumer recall noticesReference notice · device
There is an error in the product description on the Unique Device Identification (UDI) label. These discrepancies in labeling do not align with the approved product or product specifications and may lead to incorrect product identification or selection, potentially resulting in use with an incompatible bed frame.
Deerfield, IL, US · Updated 9/24/2026, 12:00:00 AM UTC
Source: FDA — device enforcement referenceReference notice · consumer
This recall involves Aitjunz 8-Drawer Dressers. The recalled dressers come in black, white, brown, oak and cream. The dressers have eight drawers and are made from wood. They measure 15.55 inches wide, 55.11 inches long, 30.78 inches tall and weigh 129 pounds. SKU “LDQMFJ8D-BR,” “LDQMFJ8D-CM,” “LDQMFJ8D-WH,” “LDQMFJ8D-…
US · Updated 9/24/2026, 12:00:00 AM UTC
Source: CPSC — consumer recall noticesReference notice · device
There is an error in the product description on the Unique Device Identification (UDI) label. These discrepancies in labeling do not align with the approved product or product specifications and may lead to incorrect product identification or selection, potentially resulting in use with an incompatible bed frame.
Deerfield, IL, US · Updated 9/24/2026, 12:00:00 AM UTC
Source: FDA — device enforcement referenceReference notice · consumer
These recalled products are packaged in a large clear plastic bag. A white label on the clear plastic bag has, in black font, one of the following identifiers: 6502 (for the light-up tie), HD-10 (for the light-up headbands) or L-508 (for the light-up glasses). Each of the items are packaged in individual clear plastic …
US · Updated 9/24/2026, 12:00:00 AM UTC
Source: CPSC — consumer recall noticesReference notice · consumer
This recall involves Emerspring Mattresses. The mattresses are 12 inches thick and sold in queen size. They have a white top and white sides with a green trim. They were sold compressed in a box. “Prototype ID: EMERS-12” and the manufacture date “6/2025” are printed on a sewn-in white label located on one side of the m…
US · Updated 9/24/2026, 12:00:00 AM UTC
Source: CPSC — consumer recall noticesReference notice · consumer
This recall involves Kesyup-branded Mattresses. They are 12 inches thick and were sold in twin, full, queen and king sizes. They have a white top and blue sides with blue trim. The mattresses were sold in compressed boxes. “Prototype ID: PU-US” is printed on a sewn-in white label on one side of the mattress.
US · Updated 9/24/2026, 12:00:00 AM UTC
Source: CPSC — consumer recall noticesReference notice · consumer
This recall involves the portable sleep machine which features various sounds, adjustable volume, a built-in nightlight, and includes a USB charging cable. “Love to Dream” is imprinted on the sleep machine and on the brown handle. Only machines with model number LTD-SM23 and date code 7W15TN are included in this recall…
US · Updated 9/24/2026, 12:00:00 AM UTC
Source: CPSC — consumer recall noticesReference notice · food
Potential contamination with Salmonella.
Salinas, CA, US · Updated 9/23/2026, 12:00:00 AM UTC
Source: FDA — food enforcement referenceReference notice · food
Product may be contaminated with Salmonella
Mamaroneck, NY, US · Updated 9/23/2026, 12:00:00 AM UTC
Source: FDA — food enforcement referenceReference notice · food
Potential contamination with Salmonella.
Salinas, CA, US · Updated 9/23/2026, 12:00:00 AM UTC
Source: FDA — food enforcement referenceReference notice · food
Jalapenos have the potential to be contaminated with Salmonella
Missouri City, TX, US · Updated 9/23/2026, 12:00:00 AM UTC
Source: FDA — food enforcement referenceReference notice · food
Jalapenos have the potential to be contaminated with Salmonella
Missouri City, TX, US · Updated 9/23/2026, 12:00:00 AM UTC
Source: FDA — food enforcement reference