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. 2,619 recalls have been distributed to Maryland in the last 12 months.
Showing 39801–39820 of 52,535 recalls
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to A gradient cable in the ACGD...
The Issue: A gradient cable in the ACGD cabinet may be missing a spacer that prevents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HardyCHROM MRSA Cat no: G307 Lot no: H15155 Expires: 2015-08-13 Recalled by...
The Issue: Hardy Diagnostics is recalling HardyCHROm MRSA due to a report of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micro-Mate Tuberculin Glass Syringe Recalled by Cadence Inc. Due to...
The Issue: Graduation marks of the syringe are not centered with the numeric position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfectum Tuberculin Glass Syringe Recalled by Cadence Inc. Due to...
The Issue: Graduation marks of the syringe are not centered with the numeric position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Electrical Clipper with Charging base The Electrical Surgical...
The Issue: Charging base of surgical clippers overheats and smokes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitroglycerin Transdermal System 0.2 mg/hr (10 cm2) Recalled by Kremers...
The Issue: Failed Impurities/Degradation Specifications: failed specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nitroglycerin Transdermal System 0.4 mg/hr (18 cm2) Recalled by Kremers...
The Issue: Failed Impurities/Degradation Specifications: Two lots failed specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Westbrook's Hot Dilly Beans Recalled by Westbrook's Cannery Due to Products...
The Issue: Products potentially underprocessed.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: WESTBROOK'S CANNERY HORSERADISH DILL PICKLES Recalled by Westbrook's Cannery...
The Issue: Products potentially underprocessed.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: WESTBROOK'S CANNERY HOT DILL PICKLES Recalled by Westbrook's Cannery Due to...
The Issue: Products potentially underprocessed.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: West brook's Dilly Beans Recalled by Westbrook's Cannery Due to Products...
The Issue: Products potentially underprocessed.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: WESTBROOK'S CANNERY DILL PICKLES Recalled by Westbrook's Cannery Due to...
The Issue: Products potentially underprocessed.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Westbrook's Horseradish Dilly Beans Recalled by Westbrook's Cannery Due to...
The Issue: Products potentially underprocessed.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheter 14 Fr in the...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S4C Occiput Torque Wrench F/Set Screw Recalled by Aesculap, Inc. Due to A...
The Issue: A FW103R torque wrench that was improperly reassembled after reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadiForce RX850 Recalled by Eizo Corporation Due to EIZO is recalling the...
The Issue: EIZO is recalling the RadiForce LCD Monitors could display abnormally while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.