Consumer Product Recalls

Hazard: Vehicle lights that fail to illuminate can decrease visibility and increase the risk of a crash.

Hazard: A damaged cable can short circuit, increasing the risk of a fire.

Hazard: A detached idler gear can damage the engine, resulting in a stall and increasing the risk of a crash or injury.

Hazard: A detached idler gear can damage the engine, resulting in a stall and increasing the risk of a crash or injury.

Hazard: An incorrectly displayed warning light can fail to alert the driver to critical safety information, increasing the risk of a crash.

Hazard: Unintended boom movement increases the risk of injury.

Hazard: A broken side plate may result in pedestal and truck frame separation, increasing the risk of injury.

Hazard: An incorrect weight rating may lead to unintentionally overloading the vehicle, increasing the risk of a crash.

Hazard: An overloaded vehicle can increase the risk of a crash. Vehicles with incorrect wheel and tire information may lead to tires that are inflated improperly, which can also increase the risk of a crash.

Hazard: The plastic zip tie used with the recalled furniture tip kits can become brittle or break, which can allow a clothing storage unit that is anchored to the wall to detach during a furniture tip-over event, posing a tip-over and entrapment hazard that can result in death or serious injuries to children.

Hazard: The recalled roller shades have long operating cords that can cause death or serious injury to children, due to strangulation and entanglement hazards. The window coverings are in violation of the federal regulations for window coverings and present a substantial product hazard. The shades also violate labeling requirements for window coverings.

Hazard: The glow sticks and glasses violate the mandatory federal battery-operated toy regulation because the button cell batteries are in a compartment that can be opened easily without requiring the use of a common household tool. When button cell and coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns or death, posing an ingestion hazard to children.

Hazard: The swings pose a suffocation risk because they were marketed for infant sleep, and they have an incline angle greater than 10 degrees, in violation of the Safe Sleep for Babies Act. In addition, the swings fail to meet mandatory warning requirements under the swing standard and are missing the required warnings and instructions for consumer products containing button cell and coin batteries under Reese's Law.

Hazard: The lithium-ion battery in the recalled power banks can overheat and ignite, posing fire and burn hazards to consumers.

Hazard: The hook of one boot can catch on the lace of the other boot, posing a fall hazard to the consumer.

Hazard: Incorrect software flagging may occur for the assay that may potentially lead to an erroneous result.

Hazard: Due to a software issue, when attempting to restock the automated dispensing cabinet, user have received the banner message "Stocking window has passed, or item has been removed from purchase order. Please contact Pharmacy for assistance". When this occurs, the medication cannot be restocked and can potentially lead to delays in accessing medication for patients.

Hazard: Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.

Hazard: Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.

Hazard: Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.

Hazard: Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.

Hazard: Due to a software bug, automated dispensing cabinet is unable to calculate countback discrepancies during the issue process, which causes incorrect transaction quantity to be recorded. This bug can also result in the CUBIE opening more times than needed for the transaction to be completed, which may result in a patient receiving more than the intended dose of medication.

Hazard: DNA Labeling Kit for use in sample labeling to be hybridized to oligonucleotide microarrays has a component, Human Reference DNA Female aliquot, affected by a mosaic aberration that may result in Chromosome 12 baseline shift, which may lead to false positive/negative results, resulting in diagnosis delay, and may lead to delayed treatment of a treatable genetic disorder.

Hazard: There is a software issue that can permanently disable communication with an implantable neurostimulator (INS) when a specific intraoperative programming sequence is used.

Hazard: Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.

Hazard: Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.

Hazard: Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.

Hazard: Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.

Hazard: Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.

Hazard: Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.