Latest Product Recalls Today

This recall involves Favoto Model H-1 bike helmets. The helmet body is black with red stripes, black padding, black straps with a silver reflective pattern in the center and a black and red buckle with a black chin strap. The recalled helmets were sold in youth size large (L). The helmets have a black plastic knob at the back of the helmet for adjusting the fitting. "FAVOTO" can be found in white letters on the side of the helmet.

This recall involves EVLWZL and Gunugu Mattresses. The mattresses are 10 and 12 inches thick and were sold in twin, full, queen and king size. They have a black top and sides. They were sold compressed in a box. The fiber content, size and "WG/P Foundation" are on a white label sewn onto the mattress cover. EVLWZL is on a black sewn on label on the front side.

This recall involves EEMB lithium batteries in individual pouches, models include: CR2025, CR2032, CR2450, CR2477, CR2016, CR1220, CR1225, CR1616, CR1620, CR1632 and CR2025-10. The lithium coin batteries come in a five, ten or twenty size pack. "EEMB" and the battery type is printed on the face of the coin battery. The white pouch has "EEMB" printed in the upper left corner.

This recall involves all Analemma-branded water bottles. The stainless-steel water bottles were sold in black or white and have a glass inner liner and a screw-on top. The Analemma logo, "24 oz" and "Analemma The Architect of Life" are printed on the front of the water bottles.

This recall involves youth sweatshirts with drawstrings. The sweatshirts are gray and have the Bobcat name and logo printed in black on the chest of the sweatshirt. The sweatshirts were sold in youth sizes 8/10 and 12/14. The size of the sweatshirt and "RN#36753" is printed on the neck label in black.

product tested positive for Listeria Monocytogenes.

Undeclared food colorings (Yellow 6, Blue 1, and Yellow 5) and unapproved Acid Red 14.

Product contains undeclared Yellow No. 5.

Foreign object found inside retail container.

Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).

Undeclared allergen (almond).

Product may contain foreign objects, specifically glass.

Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).

Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).

Contains undeclared FD&C Yellow 6

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

Ten complaints have been received identifying issues at the time of use related to the package seal, including incomplete seals, wrinkles in the seals or peeling seals. Compromised sterile barrier may lead to clinically insignificant extension of surgery or infection leading to surgical intervention.

Due to complaints of device breakage at the traction force gauge to handle joint.