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.

52,535 total recalls
2,877 in last 12 months

Showing 46614680 of 29,093 recalls

Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion DISP.UMBILICAL CORD CLAMP CUTTER(CTR300) Recalled by MEDLINE...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion manual surgical kits labeled as: a) STERILE 4-1/2" S/S Recalled by...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation Software Version Numbers version numbers 8B Recalled by RAYSEARCH...

The Issue: A use error that has occurred with RayStation/RayPlan, where material...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion retractor kits labeled as: a) STERILE 6-1/2" SENN RETRACTOR...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion Clamp kits labeled as: a) STERILE BACKHAUS TOWEL CLAMP (BTC173)...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE 4.5 IN WIRE CUT SCISSORS Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE SWABSTICKS PVP 3 PK Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion STERILE #16 RUBBER BAND Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· Human Care Hc Sweden Ab

Recalled Item: Altair 330 lbs w/o Hanger Bar Recalled by Human Care Hc Sweden Ab Due to...

The Issue: Patient lift hanger bar may come loose, which could potentially pose risks...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion FCP MAGILL CATH 7.5 IN PED (67575) Recalled by MEDLINE INDUSTRIES,...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Juniper Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: On ultrasound systems, when Cardiac DICOM SR feature is configured to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Maple Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: On ultrasound systems, when Cardiac DICOM SR feature is configured to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion Forcep kits labeled as: a) STERILE F/P SPLINTER FORCEP (SF6141)...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2024· Baxter Healthcare Corporation

Recalled Item: Surgical Tools and Cardiovascular Specialty marketing brochures Recalled by...

The Issue: The Surgical Tools and Cardiovascular Specialty marketing brochures...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2024· Bolton Medical Inc.

Recalled Item: RELAY PRO Thoracic Stent-Graft System Recalled by Bolton Medical Inc. Due to...

The Issue: The stent-graft inside the delivery system was the incorrect size.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2024· Baxter Healthcare Corporation

Recalled Item: Surgical Tools and Cardiovascular Specialty marketing brochures Recalled by...

The Issue: The Surgical Tools and Cardiovascular Specialty marketing brochures...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2024· Baxter Healthcare Corporation

Recalled Item: Surgical Tools and Cardiovascular Specialty marketing brochures Recalled by...

The Issue: The Surgical Tools and Cardiovascular Specialty marketing brochures...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Covidien

Recalled Item: Situate Laparotomy Sponge Recalled by Covidien Due to Packs including 5...

The Issue: Packs including 5 laparotomy sponges may contain incorrect product with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Abbott Laboratories

Recalled Item: ARCHITECT STAT Myoglobin Reagent Kit Recalled by Abbott Laboratories Due to...

The Issue: The reason for the recall is the failure of calibration and quality controls...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Bruder Healthcare Company, LLC

Recalled Item: Thermalon Sinus Compress (French) Recalled by Bruder Healthcare Company, LLC...

The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...

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

Class II — Potential Health HazardOngoing