Product Recalls in Maryland
Product recalls affecting Maryland — including food, drugs, consumer products, medical devices, and vehicles distributed to Maryland. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,685 recalls have been distributed to Maryland in the last 12 months.
Showing 23501–23520 of 52,535 recalls
Recalled Item: BD Vacutainer PST Gel and Lithium HeparinN (LH) 83 Units Blood Collection...
The Issue: False elevation of carboxyhemoglobin (COHb) results have been reported when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis FA Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A tolerance issue in the power supply of the generator control above a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis dBC Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A tolerance issue in the power supply of the generator control above a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Testosterone Topical Solution 30mg of testosterone per pump actuation *...
The Issue: Defective Container; actuator may improperly function and affect dose delivery.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SYNCHRON Systems Barbiturates Reagent (BARB 1 X 250) Recalled by Beckman...
The Issue: The firm has identified that cross-reactivity testing may not meet the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CTSTM Essential 8 Medium Recalled by Life Technologies Corporation Due to...
The Issue: Component was not tested by the supplier for adventitious agents
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StemPro¿ MSC SFM CTS" Recalled by Life Technologies Corporation Due to...
The Issue: Component was not tested by the supplier for adventitious agents
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Human Assayed Multi-Sera Level 2 Recalled by Randox Laboratories, Limited...
The Issue: The RX Series control target and range value for ALT (Tris buffer without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luer Lock Set - Catalog # MPC-125 Recalled by Molded Products Inc Due to...
The Issue: Mislabeling - Some unit of sale packages (bags of 100 sets of MPC-125) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Reverse Shoulder Instrument Case Outer (Outer Case Vault Only)...
The Issue: Lack of an adequate sterilization validation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X Recalled by Philips Medical Systems (Cleveland) Inc Due to An...
The Issue: An issue with the handcontroller may result in either spontaneous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Recalled by Philips Medical Systems (Cleveland) Inc Due to An...
The Issue: An issue with the handcontroller may result in either spontaneous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus WM-NP2 or WM-DP2 Mobile Workstations with Nurse Control Panel Arm...
The Issue: WM-NP/DP2 workstations could become unstable and may fall over if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Reverse Shoulder Instrument Case Total (Outer Case Vault Only)...
The Issue: Lack of an adequate sterilization validation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity ci -series System Control¿Module Recalled by Abbott Gmbh & Co. KG...
The Issue: Abbott has identified an issue with all on market versions (v2.6.0 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView SPECT Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: An issue with the handcontroller may result in either spontaneous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vest Recalled by Burlington Medical, LLC Due to The protective material used...
The Issue: The protective material used in the manufacture of the products could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cap Recalled by Burlington Medical, LLC Due to The protective material used...
The Issue: The protective material used in the manufacture of the products could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Overlap Vest Recalled by Burlington Medical, LLC Due to The protective...
The Issue: The protective material used in the manufacture of the products could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peak Vest Recalled by Burlington Medical, LLC Due to The protective material...
The Issue: The protective material used in the manufacture of the products could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.