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. 2,877 recalls have been distributed to Maryland in the last 12 months.
Showing 4381–4400 of 29,093 recalls
Recalled Item: Medline medical procedure kits labeled as follows: a) KIT CANISTER Recalled...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits labeled as follows: DENTAL Recalled by...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1500ML SOFT LINER Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to A...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits labeled as follows: a) ENDO KIT Recalled by...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits labeled as follows: a) BASIC NEURO Recalled...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits labeled as follows: a) ANESTHESIA CIRCUIT...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits labeled as follows: a) GYN CDS Recalled by...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits labeled as follows: a) ENDO KIT Recalled by...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits labeled as follows: a) C-SECTION CDS Recalled...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits labeled as follows: a) MAJOR BREAST Recalled...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits labeled as follows: a) ARTHROSCOPY Recalled...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 48" Lead Wires Recalled by EBI, LLC Due to Damage to the lead wire sheath...
The Issue: Damage to the lead wire sheath (black cable) component and causing exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet SpinalPak Non-invasive Spine Fusion Stimulator System- Indicated for...
The Issue: Damage to the lead wire sheath (black cable) component and causing exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Redux Electrolyte Creme Recalled by Parker Laboratories, Inc. Due to Product...
The Issue: Product demonstrates low viscosity.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Patient Information Center (PIC) iX Uninterruptable Power Supply...
The Issue: Possible failure of Uninterruptable Power Supply (UPS) devices supporting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20" Lead Wires Recalled by EBI, LLC Due to Damage to the lead wire sheath...
The Issue: Damage to the lead wire sheath (black cable) component and causing exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet OrthoPak Non-invasive Bone Growth Stimulator System-Indicated for the...
The Issue: Damage to the lead wire sheath (black cable) component and causing exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AW-S025 NEO SONARMED SENSOR 2.5MM. Used in conjunction with SonarMed...
The Issue: The failure to detect the partial obstruction in a 2.5mm sensor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AW-S030 NEO SONARMED SENSOR 3.0MM. Used in conjunction with SonarMed...
The Issue: The failure to detect the partial obstruction in a 2.5mm sensor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AW-S035 NEO SONARMED SENSOR 3.5MM. Used in conjunction with SonarMed...
The Issue: The failure to detect the partial obstruction in a 2.5mm sensor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.