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. 2,882 recalls have been distributed to Maryland in the last 12 months.
Showing 4341–4360 of 52,535 recalls
Recalled Item: SE GROCERS 12/16.5oz GRDL PNCK HSTYLE-SEGGR PICS BY Recalled by Treehouse...
The Issue: potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KODIAK CAKES 8/10.72oz GRDL WFL DRKCH Recalled by Treehouse Foods Due to...
The Issue: potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KODIAK CAKES 8/13.40oz GRDL WFL BTRMLK VAN-KDKCS Recalled by Treehouse Foods...
The Issue: potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SELECTION 1/1.68kg GRDL WFL CHOC CHIP-SLCTN NO NAME Recalled by Treehouse...
The Issue: potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HANNAFORD 8/12.3oz GRDL WFL MLTGRN-HANNA FOODHOLD 8/12.3oz GRDL Recalled by...
The Issue: potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Perio Maintenance Rinse 0.63% Stannous Fluoride Concentrated Solution...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Member's Mark Hatch Chile Chicken Enchiladas Recalled by Sam'S Club Due to...
The Issue: Presence of Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CorNeat EverPatch Recalled by CORNEAT VISION, LTD. Due to Retroactive; Due...
The Issue: Retroactive; Due to complaints, labeling correction for permanent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) COMBINED SPINAL AND EPIDURAL...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smaxel Fractional CO2 Laser Recalled by IDS LTD Due to The Smaxel Fractional...
The Issue: The Smaxel Fractional CO2 Laser does not include a Certification label, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) CONT EPI 20G W/HUSTEAD...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) 20G EPI CATH SINGLE STERILE...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) ECHOSTIM BLOCK SET Recalled by...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) PERIPHERAL CONTINUOUS NERVE BL...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) L&D CONTINUOUS EPIDURAL TRAY...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) NEURAXIAL KIT Recalled by...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE NEXUS 19/20G CATH CONNECTOR Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acrobat-i Vacuum Stabilizer System. Model Number C-OM-10000Z Recalled by...
The Issue: Deviations in the manufacturing process created a compromise in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acrobat SUV Vacuum Stabilizer System Recalled by Maquet Cardiovascular, LLC...
The Issue: Deviations in the manufacturing process created a compromise in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acrobat-i Positioner. Model Number C-XP-5000Z Recalled by Maquet...
The Issue: Deviations in the manufacturing process created a compromise in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.