Alabama recalls

Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which may result in the backup alarm not activating during loss of primary power and absence/depletion of backup power sources, which may result in delayed caregiver awareness of a hazardous condition.

Custom temporomandibular joint implant may have contained incorrect patient-specific components that led to a poor fit of the implant, leading to a right-sided open bite.

Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker output.

Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker output.

Operative components of surgical systems potentially distributed with E-brake retainer pin, so in event of a structural column failure, the E-brake pin would prevent E-brake engagement and may result in uncontrolled motion. In addition, if it moves/backs out it may cause restricted column range of motion and/or uncontrolled motion, which may cause patient tissue injury/crushing injury/bleeding.

The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.

The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.

The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.

The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.

Undeclared allergens: Milk and Soy

The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

Potential presence of Salmonella.

Potential presence of Salmonella.

Potential presence of Salmonella.

Potential presence of Salmonella.

Potential presence of Salmonella.

Potential presence of Salmonella.

Potential Salmonella contamination

Potential Salmonella contamination

Potential Salmonella contamination

Potential Salmonella contamination

Potential Salmonella contamination.

Potential Salmonella contamination.

Potential Salmonella contamination

Potential Salmonella contamination