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. 2,782 recalls have been distributed to Maryland in the last 12 months.
Showing 17281–17300 of 29,093 recalls
Recalled Item: Alden Classic 55 Toric Daily Wear Soft contact Recalled by Alden Optical Due...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP54 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi Beaver Optimum Safety Sideport Knife: (a) Straight 15o Recalled by...
The Issue: The protective shield was retracted, and the blade was exposed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP54 Sphere Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP59 Sphere Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASTERA Multifocal Toric Daily Wear Soft contact Recalled by Alden Optical...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi Beaver Safety Sideport Knife: (a) 1.0mm Recalled by Beaver-Visitec...
The Issue: The protective shield was retracted, and the blade was exposed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi Beaver EdgeAhead Safety Knife Recalled by Beaver-Visitec International...
The Issue: The protective shield was retracted, and the blade was exposed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Everflex Self-Expanding Peripheral Stent with Entrust Delivery System...
The Issue: Stent length on the label may not match the length of the stent itself.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Imaging System s5i Recalled by Volcano Corporation Due to On certain...
The Issue: On certain Impacted Systems, an unexpected Microsoft Windows Security dialog...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: pmi Recalled by Pro-Med Instruments Gmbh Due to The firm received reports of...
The Issue: The firm received reports of two breakages of the pin tips which occurred...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CM0405 Mueller-Hinton Broth IVD Recalled by Remel Inc Due to Product may...
The Issue: Product may have incorrect cation information detailed on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACE(TM) BRAND Recalled by 3M Company - Health Care Business Due to Mold was...
The Issue: Mold was found on the non-patient contact surfaces of the product and was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to The internal...
The Issue: The internal configuration of the electrometers and the Real-Time control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Mednet(TM) Medication Management Suite 6.1 and 6.21 Recalled by ICU...
The Issue: Issue 1: The MedNet Meds 6.1 and 6.21 programs, under certain conditions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum 360 Infusion System Recalled by ICU Medical Inc Due to (1) Under...
The Issue: (1) Under certain conditions, if a malfunction alarm occurs while the pump...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: fMRI Hardware System - AudioSystem Recalled by NordicNeuroLab AS Due to...
The Issue: Report was of an interrupted MR scan after patient complained about acoustic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK(R) Electrode Starter Kits Recalled by Physio-Control, Inc. Due to...
The Issue: The infant artwork on the product instructs incorrect pad placement. Also,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK(R) defibrillation electrodes Recalled by Physio-Control, Inc. Due to...
The Issue: The infant artwork on the product instructs incorrect pad placement. Also,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L3 Security & Detection System Cabinet X-ray system used for Recalled by L3...
The Issue: L3 has determined in airport environments, there have been several cases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.