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. 945 recalls have been distributed to Maryland in the last 12 months.
Showing 44421–44440 of 52,535 recalls
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gel-E Donut Recalled by Childrens Medical Ventures Due to The gel-filled...
The Issue: The gel-filled Gel-E Donut and Squishon product line has received a number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abacus 3.1 Recalled by Baxter Corporation Englewood Due to Baxter...
The Issue: Baxter Corporation is initiating a field correction following an upgrade to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navitas Naturals Omega Blend Sprouted Smoothie Mix Recalled by Navitas,...
The Issue: Data obtained from interviews of patients in a multistate outbreak of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: William & Sonoma Navitas Naturals brand Omega 3 Smoothie Mixer Recalled by...
The Issue: Data obtained from interviews of patients in a multistate outbreak of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Navitas Naturals Organic Sprouted Chia Powder Recalled by Navitas, LLC., dba...
The Issue: Data obtained from interviews of patients in a multistate outbreak of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Large Pitted Kalamata Olives Recalled by Dot Foods Inc. Due to This...
The Issue: This voluntary recall has been initiated because Savor Brands Large Pitted...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FirmArray Blood Culture Identification (BCID) Panel Recalled by BioFire...
The Issue: BioFire has identified an increased risk of false positive results when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Langston Dual Lumen Catheters Recalled by Vascular Solutions, Inc. Due to...
The Issue: The inner catheter of some Langston V2 Dual Lumen Catheters have separated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Recalled by Teleflex Medical Due to Although the Natural Rubber Latex...
The Issue: Although the Natural Rubber Latex caution symbol is clearly displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSI Cardiovascular Systems Recalled by Cardiovascular Systems, Inc. Due to...
The Issue: CSI has initiated a recall on the Diamondback 360 Peripheral Orbital...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Flexible Aortic Arch Cannula 8.0mm with luer Recalled by Terumo...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Venoatrial Cannulae 36/46 Fr with 1/2" flare or connector Recalled by...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Three-stage Venous Return Cannulae 28 Fr with 3/8" flare Recalled by...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDPoint 500 Measurement Clinical Chemistry System RAPIDPoint 500...
The Issue: RAPIDPoint 500 Measurement Cartridges may have an error code one or more...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPB Catheter Kit Product Usage: Venous Return Cannula is indicated Recalled...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.