At PHS, your safety is our top priority. Below, you’ll find important updates on product recalls, safety notices, and product updates to ensure you have the latest information about your products. For question contact your local branch.
Updated 12/8/2025
Medline Industries, LP has notified PHS of an Urgent Medical Device Product Recall for specific lot(s) of Hudson RCI Medium Concentration Oxygen Masks. This notice has been issued due to complaints that the oxygen tubing is disconnecting with certain models.
Updated 12/4/2025
Medline Industries, LP has notified PHS of an Urgent Medical Device Product Recall for specific lot(s) of Hudson RCI Medium Concentration Oxygen Masks. This notice has been issued due to complaints that the oxygen tubing is disconnecting with certain models.
Updated 11/6/2025
BD has notified McKesson Medical-Surgical Inc. (MMS) of an Urgent Medical Device Product Removal due to certain BD Luer Tip Cap trays that failed routine testing. The products affected first shipped March 14, 2025.
Updated 9/18/2025
Convatec has notified McKesson Medical-Surgical Inc. (MMS) of an Urgent Product Recall regarding one lot of Duoderm Xtra Thin Dressings. This notice is a result of a customer complaint regarding a foreign matter on a product.
Updated 9/9/2025
DermaRite has notified McKesson Medical-Surgical Inc. (MMS) of an Urgent Product Recall regarding all lots of various DermaRite products. This notice has been issued because the presence of microbial levels are above the FDA recommended amount and poses a risk of localized skin irritation.
Updated 8/14/2025
We wanted to inform you that McKesson Medical-Surgical Inc. (MMS) has notified PHS of an Urgent Product Recall regarding MediHoney Wound & Burn products. As stated in the Product Notice: “This notice has been issued because packaging failures were identified which could lead to a breach in the sterile barrier.” The affected product first shipped on July 14, 2021.
Updated 7/29/2025
McKesson has notified PHS of an Urgent Field Safety Notice regarding specific lots of the SPUR Resuscitator variants. This recall was issued because, Ambu received five reports that the SPUR II device may have a blocked manometer port, causing the manometer to not function properly.
Read Recall Notice Patient Letter
Updated 6/30/2025
Medtronic has issued a safety notification for its Covidien Nellcor Bedside SpO2 Patient Monitoring System. This safety notification serves as a reminder to ensure that alarms are audible throughout the home.
Read Safety Notice Patient Letter
Updated 6/12/2025
We’re pleased to inform you that the manufacturer has resumed regular production, and we will be returning to our standard shipment of 30 bags per month.
Updated 5/22/2025
Vesco Medical has notified PHS of an Urgent Medical Device Recall regarding their ENFit Medicine Bottle Adapters. This recall was issued because, it has been determined that some of the male fitting adapters do not fit into the accompanying syringe. There have been no reports of patient adverse effects resulting from this fitting issue.
Updated 4/29/2025
PHS has been informed about a Voluntary Medical Device Recall from Resmed for specific lot(s) of their AirFit F20 Non Magnetic Full Face Mask. In some lot(s) there is magnetic frame placed in the system package making the mask unusable. To date there have been no adverse effects reported
Updated 4/17/2025
PHS was notified through McKesson Medical-Surgical Inc, of an Urgent Medical Device Recall from Airlife regarding their reusable blood pressure cuffs. This notice has been issued because the product is labeled “not made with natural rubber latex,” however, there is a latex-containing rubber band located around the product instructions for use (IFU). Affected product first shipped June 1, 2021.
Updated 4/3/2025
PHS was notified through McKesson Medical-Surgical Inc, of an Urgent Medical Device Notice from Airlife regarding specific lot(s) of four Ballard Closed Suction Systems. This notice has been issued due to the fact that the product shipped was not sterilized through their standard gamma radiation process. Affected product first shipped January 9, 2025.
Updated 2/25/2025
PHS was notified through Smiths Medical, of an Urgent Product Recall regarding BCI Airway Adapters that are supplied individually and/or in certain kits. As stated in the Urgent Product Recall from the Manufacturer: “Investigation determined that the weld between the mating parts may not meet specifications.”