Latest Product Recalls Today

Undeclared Milk, Eggs, Yellow #5.

Undeclared Red #40, Blue #1, Blue #2

Undeclared Milk, Walnuts, Eggs, Wheat, Soy.

Undeclared Milk, Wheat, Soy, Yellow #5, Green #3.

Undeclared Soy (with mitigating circumstances)

Potential contamination with pesticides, haloxyfop and thiamethoxam

Potential Salmonella contamination. The firm was notified from their supplier that the nonfat dry milk may be contaminated with Salmonella.

Potential contamination with Salmonella.

Undeclared Milk, Red #40.

Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic.

Product has the potential to be contaminated with Salmonella.

Potential contamination with foreign materials.

Package integrity compromised.

Multi-state outbreak of E. coli O157:H7.

Potential contamination with Salmonella.

Undeclared Milk, Soy, Red #40.

Undeclared Yellow #5

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated with device fragmentation/separation, and vessel injury. In a worst-case scenario, device fragmentation and separation may cause life-threatening harm or death.

Respiratory/sore throat panel test may result in false negative results and control failures.

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

If the connection between a mint Lesion workstation and the mint Lesion server is interrupted while performing a read, in rare cases some information may be lost or incorrectly linked to other patients.

Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated with device fragmentation/separation, and vessel injury. In a worst-case scenario, device fragmentation and separation may cause life-threatening harm or death.

Reloads for curved-tipped stapler may potentially produce an incomplete staple line.

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.