All Recalls

Karman Healthcare, Inc. is recalling Karma Flexx Wheelchair because incorrect size screws and corresponding hardware were installed on the front caster fork brackets.

During an evaluation of the product packaging, it was determined that there is a potential for the product to cause damage to the packaging, creating a possible breach in sterility.

8FR 16 PVC tubes were packaged in a 6.5 FR 36 Polyurethane packs and 8FR 20 PVC tubes were packaged in an 8FR 20 Polyurethane packs

During an evaluation of the product packaging, it was determined that there is a potential for the product to cause damage to the packaging, creating a possible breach in sterility.

The incorrect sheath was assembled to the device so that the size 7 products received 11 cm sheaths and the size 11 product received 7 cm sheaths.

Complaints were received claiming the material failed to polymerize under the curing light. After investigation, it was determined that a wrong photo-initiator was used in the production batch U30755 of Helioseal Clear. This failure can lead to incomplete curing of the sealant, if mono-wave LED curing lights are used.

MAQUET Medical Systems USA is initiating a field action for correction of the MAQUET Extension Device (Part No 1180.19F0). The Extension Device is manufactured by Maquet GmbH, in Germany, and is a table top module for use with the Maquet MAGNUS operating table system. Maquet GmbH was made aware of a potential issue that can result in the Extension Device becoming unlocked from the table top, causing it to fall down.

The batteries inside the clock can overheat due to defective battery springs located at the bottom of the battery compartment, posing a fire hazard.

The decorative wall plates can dislodge from the backplate and short circuit the outlet, posing a risk of electrical shock or fire.

The battery packs in the flashlights can overheat, posing a fire hazard to consumers.

Recent FDA analysis determined that the product is decomposed and was also identified as Spanish mackerel.

Great Pacific Bagel & Cream Cheese was recalled due to undeclared wheat

IEH sampling found samples of raw macadamia nuts to be positive for Salmonella.

This voluntary recall was initiated after the manufacturing firm notified the recalling firm that products were possibly under- processed. Under-processed seafood could lead to contamination with Clostridium botulinum.

Roundy's is recalling Simply Roundy's Natural Authentic Italian Sweet Butternut Squash Ravioli because the product may contain undeclared cashew and almond. This product was manufactured and recalled by Bertagni 1882 SpA of Arcugnano, Italy due to undeclared cashews and almonds.

IEH sampling found samples of raw macadamia nuts to be positive for Salmonella.

IEH sampling found samples of raw macadamia nuts to be positive for Salmonella.

House of Flavors, Inc. is voluntarily recalling a small batch of 8 oz. cups of Purple Cow Limited Edition Cookie Butter Ice Cream, sold at Meijer stores, that contain Purple Cow Butter Pecan Ice Cream with a Purple Cow Butter Pecan lid.

Undeclared Allergens: milk, eggs, wheat and fish.