Pet food and pet product recalls

Albright’s Raw Pet Food of Fort Wayne, Indiana out of an abundance of caution is voluntarily recalling one lot of its Chicken Recipe for Dogs Complete and Balanced because this lot has the potential to be contaminated with Salmonella.

HOUSTON, TX, May 5, 2026 — CBSL Commissary LLC, operating as Winfield’s Chocolate Bar, is voluntarily recalling five dark chocolate products sold at its three Houston, Texas locations because the word “milk” was omitted from the ingredient label. Milk is a known major food allergen under the Food Al

The toys' plastic cube can break into small parts or sharp edges, posing a risk of serious injury from choking and laceration hazards.

The recalled children's toys violate the small parts ban because the toy is intended for children under three years of age and the fence handles can detach from the toy, posing a deadly choking hazard.

The recalled delivery boxes violate the mandatory standard for consumer products containing button cell and coin batteries because they contain a lithium coin battery that can be easily accessed by children, posing an ingestion hazard. The packaging also does not bear the required warning labels for products containing such batteries as required by Reese's Law. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.

Revival Animal Health of Orange City, IA is recalling Breeder’s Edge® Foster Care® Canine and Shelter’s Choice® Canine Milk Replacers due to variable levels of Vitamin D resulting in both low and elevated levels in some of the canine milk replacers.

The Montessori toy sets contain an airplane shaped teething toy that has tentacle ends that can pose a choking hazard to young children. The toys also violate the teething toy provision of the mandatory standard for children's toys.

The recalled toys violate the small parts ban because the toys are intended for children under three and the toys' xylophone screws and clock hands can detach. In addition, the toys violate the mandatory safety standard for children's toys because the mallets have spherical ends, posing a choking hazard.

The Pet Vet Playset violates the mandatory standard for toys because the button cell batteries in the nail grinder and otoscope can be easily accessed by children.

The recalled infant walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step, posing a risk of serious injury or death due to a fall hazard.

The recalled children's flashcard toy sets contain levels of lead that exceed the federal lead content ban and levels of phthalates that exceed the federal phthalates ban. Lead and phthalates are toxic if ingested by young children and can cause adverse health issues. In addition, the flashcards also violate the mandatory standard for toys because they fail to comply with the short circuit protection requirement for battery-operated toys.

The pens in the recalled children's handwriting kits contain levels of lead in the nib that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse health issues.

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

Due to damage to outer tray that can potentially compromise the sterile barrier

The recalled sleepwear violates the mandatory flammability standard for children's sleepwear, posing a risk of burn injuries to children.

Products contain banned color, carmoisine and undeclared FD&C Yellow 5 and FD&C Red 40

Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).

Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).

Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).

Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).

Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).

Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).

Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).

There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.

The legs of the plush toy can detach from the body allowing the release of small beads that are on the legs, posing a choking hazard to young children.

There is a potential intermittent issue on certain Omni Legend systems that can result in a streaking artifact in the PET clinical scan images. This streaking artifact is most easily identified in transaxial slices on the acquisition console (both corrected and non-corrected for attenuation).

The recalled baby loungers violate the mandatory safety standard for Infant Sleep Products. The sides are too low to contain an infant and the enclosed openings at the foot of the loungers are wider than allowed, posing serious risks of fall and entrapment hazards to infants. In addition, the baby loungers do not have a stand, posing a fall hazard if used on elevated surfaces. These violations create an unsafe sleeping environment and can cause death or serious injury to infants.

Treatment reagent functionality in respiratory specimens fluidification cannot be guaranteed.

Treatment reagent functionality in respiratory specimens liquification cannot be guaranteed.

Distribution without premarket approval/clearance.