All Recalls

Potential plastic pieces in the product.

Undeclared allergen: Milk. Undeclared color additives: FD&C red #40, red #6, red #5, yellow #5.

Undeclared allergen: Milk. Undeclared color additives: FD&C yellow #5, yellow #6, red #40.

Undeclared allergen: Milk. Undeclared color additives: FD&C red #40, red #6, red #5, blue #1, and yellow #5.

Undeclared allergen: Milk, tree nuts, peanuts, soy, and wheat.

Undeclared allergens: Milk, Tree Nuts, Peanuts, and Soy.

Undeclared allergen: Milk. Undeclared color additives: FD&C yellow #5, yellow #8, red #40.

Undeclared allergens: Milk and tree nuts. Undeclared color additive: FD&C blue #1.

Sub-ingredients not declared for sunflower butter.

Sub-ingredients not declared for sunflower butter.

Undeclared allergen: Milk. Undeclared color additives: FD&C yellow #5, yellow #6, red #40.

Sub Potent and Super Potent Product: During an impact assessment of the DOP Hand Sanitizer product, it was identified that several lots distributed did not comply with the finished good acceptance criteria established.

Sub Potent and Super Potent Product: During an impact assessment of the DOP Hand Sanitizer product, it was identified that several lots distributed did not comply with the finished good acceptance criteria established.

Sub Potent and Super Potent Product: During an impact assessment of the DOP Hand Sanitizer product, it was identified that several lots distributed did not comply with the finished good acceptance criteria established.

cGMP Deviations

Instructions for Use (IFU) for the Atrium Ocean, Oasis, and Express chest drains do not provide sufficient precaution instruction for proper set up of catheter(s) and patient tube connections with single collection chamber chest drains

This recall is part of a 2-issue recall for the same system. When using the IVC needle position button, on the IVC control box during a series of scans, the plan box may not move to the desired needle position. This issue could result in the gantry moving to a location the operator does not expect. If this occurs, it presents a risk that the scan could occur at an incorrect location, or that the unintended motion of the gantry could cause a collision with the user or needle. The other part of the recall involves a software crash when the CCT foot pedal is activated (as described in RES ID93363).

Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.

Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.

For oncology users: If the user performed off-set reconstruction on CT device a shift could be observed on the contouring area of the primary and secondary images sets when using image fusion (on TPS) and incorrect coordinates may be sent to TPS system when using absolute patient marking. This may lead to incorrect radiation therapy planning and possible growth or spread of cancer due to incorrect early treatment regimen. For radiology users: If the user performed off-set reconstruction on CT devices, after multiple acquisitions, the Relate Position could be inaccurate. This could lead to incorrect diagnosis and treatment.