Class IOngoingZ-2227-2025
Philips Respironics, Inc. recalls DreamStation Auto CPAP. Non-Continuous Ventilator.
Devices may possess a programming error resulting in an incorrect device configuration.
Philips Respironics, I…PAAug 20, 2025
Recalls in Pennsylvania
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 445–456 of 581 recalls
Class IOngoingZ-2176-2025
B BRAUN MEDICAL INC recalls Microbore Extension Set with 0.2 Micron Filter. Catalog Number: V6215. for use with IV…
Label is incorrect. The product label indicates that the device contains an air eliminating filter. However, the filter utilized on this extension set is not indicated for removal of air and does not feature an air vent,…
B BRAUN MEDICAL INCPAAug 13, 2025
Class IOngoingZ-2161-2025
Draeger, Inc. recalls SafeStar 60A Plus Filter. Bidirectionally breathing system filter.
Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.
Draeger, Inc.PAAug 6, 2025
Class IOngoingZ-2160-2025
Draeger, Inc. recalls HME TwinStar HEPA Plus Filter. Bidirectionally breathing system filter.
Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.
Draeger, Inc.PAAug 6, 2025
Class IOngoingZ-2159-2025
Draeger, Inc. recalls SafeStar 55 Plus Filter. Bidirectionally breathing system filter.
Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.
Draeger, Inc.PAAug 6, 2025
Class IOngoingZ-2158-2025
Draeger, Inc. recalls SafeStar 90 Plus Filter. Bidirectionally breathing system filter.
Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.
Draeger, Inc.PAAug 6, 2025
Class IIOngoingZ-2146-2025
Olympus Corporation Of The Americas recalls Cone with Male Tubing
Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
Olympus Corporation of…PAJul 30, 2025
Class IIOngoingZ-2145-2025
Olympus Corporation Of The Americas recalls Ellik Evacuator Adapter
Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
Olympus Corporation of…PAJul 30, 2025
Class IIOngoingZ-2144-2025
Olympus Corporation Of The Americas recalls Ellik Latex Bulb
Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
Olympus Corporation of…PAJul 30, 2025
Class IIOngoingZ-2143-2025
Olympus Corporation Of The Americas recalls Ellik Evacuator. Model Number: 194. The Ellik Evacuator and adapter accessories are…
Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
Olympus Corporation of…PAJul 30, 2025
Class IIOngoingZ-2142-2025
Olympus Corporation Of The Americas recalls Tubing for Male Connector 194
Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
Olympus Corporation of…PAJul 30, 2025
Class IIOngoingZ-2141-2025
Olympus Corporation Of The Americas recalls Glass Body For 194 Ellik Evacuator. Model Number: 190A. The Ellik Evacuator and ada…
Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
Olympus Corporation of…PAJul 30, 2025