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.

52,535 total recalls
2,882 in last 12 months

Showing 43614380 of 29,093 recalls

Medical DeviceMarch 26, 2024· Philips Respironics, Inc.

Recalled Item: BiPAP A40 Ventilators: BiPAP A40 Recalled by Philips Respironics, Inc. Due...

The Issue: Potential for devices to experience interruption/loss of therapy during a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2024· Philips Respironics, Inc.

Recalled Item: BiPAP A30 Ventilator Recalled by Philips Respironics, Inc. Due to Potential...

The Issue: Potential for devices to experience interruption/loss of therapy during a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2024· Medtronic Navigation, Inc.

Recalled Item: Stealth S8 Clinical Software Application Recalled by Medtronic Navigation,...

The Issue: Due to a software issue, there is the potential for a missing digit, letter,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2024· SURGICAL SPECIALTIES

Recalled Item: POLYSIN (Polyglycolic Acid) suture Recalled by SURGICAL SPECIALTIES Due to...

The Issue: Complaints have been received with allegations of Incorrect Needle Curvature.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2024· Ossur H / F

Recalled Item: RKN130002 Recalled by Ossur H / F Due to Due to firmware issues with the...

The Issue: Due to firmware issues with the prosthetic knee, there is the potential for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2024· Ossur H / F

Recalled Item: RKNXC0005 Recalled by Ossur H / F Due to Due to firmware issues with the...

The Issue: Due to firmware issues with the prosthetic knee, there is the potential for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2024· Ossur H / F

Recalled Item: RKNXC0003 Recalled by Ossur H / F Due to Due to firmware issues with the...

The Issue: Due to firmware issues with the prosthetic knee, there is the potential for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2024· Ossur H / F

Recalled Item: RKN130003 Recalled by Ossur H / F Due to Due to firmware issues with the...

The Issue: Due to firmware issues with the prosthetic knee, there is the potential for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2024· SonarMed Inc

Recalled Item: AW-M0001 SONARMED MONITOR. Used in conjunction with SonarMed Acoustic...

The Issue: Software anomaly resulted in failure to detect a partial obstruction in 2.5...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMarch 23, 2024· Philips Ultrasound, Inc.

Recalled Item: 5000 Compact Series Ultrasound Systems Recalled by Philips Ultrasound, Inc....

The Issue: Ultrasound system with: 1) transesophageal echocardiography transducer (TEE)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: LINER Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to A slight...

The Issue: A slight dimensional variation which has the potential for increased...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: LINER Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to A slight...

The Issue: A slight dimensional variation which has the potential for increased...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits labeled as follows: a) HEART ANESTHESIA SET...

The Issue: A slight dimensional variation which has the potential for increased...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: 1 Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to A slight...

The Issue: A slight dimensional variation which has the potential for increased...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits labeled as follows: a) CYSTO 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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits labeled as follows: a) BASIC NASAL Recalled...

The Issue: A slight dimensional variation which has the potential for increased...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: 1 Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to A slight...

The Issue: A slight dimensional variation which has the potential for increased...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits labeled as follows: a) AAA 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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits labeled as follows: a) TURNOVER KIT Recalled...

The Issue: A slight dimensional variation which has the potential for increased...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: 1 Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to A slight...

The Issue: A slight dimensional variation which has the potential for increased...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing