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. 2,898 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,898 in last 12 months

Showing 22612280 of 52,535 recalls

Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: MAJOR THORACOSCOPY BASIN. Medical convenience kit. Recalled by AVID Medical,...

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: PARTIAL NEPHRECTOMY PACK. Medical convenience kit. Recalled by AVID Medical,...

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: CARDIAC ROBOT PACK. Medical convenience kit. Recalled by AVID Medical, Inc....

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: DAVINCI UROLOGY. Medical convenience kit. Recalled by AVID Medical, Inc. Due...

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: GS ENDOSCOPY PACK. Medical convenience kit. Recalled by AVID Medical, Inc....

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: CT DAVINCI. Medical convenience kit. Recalled by AVID Medical, Inc. Due to...

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: DA VINCI PACK URO/PROSTATE. Medical convenience kit. Recalled by AVID...

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· FUJIFILM Healthcare Americas Corporation

Recalled Item: ASPRIRE Cristalle Mammography System (cleared under K212873) installed with...

The Issue: Devices had an unapproved slabbing software function enabled for use.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· CooperSurgical, Inc.

Recalled Item: Endosee System Convenience Kit with IV Tube. Model Number: ES-TRAY-IV....

The Issue: The HSG Procedure Trays and Endosee System Convenience Kits contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· CooperSurgical, Inc.

Recalled Item: Endosee System Convenience Kit. Model Number: ES-TRAY. Endosee System...

The Issue: The HSG Procedure Trays and Endosee System Convenience Kits contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· CooperSurgical, Inc.

Recalled Item: HSG Procedure Tray. Model Number: 6050T. The HSG Procedure Tray Recalled by...

The Issue: The HSG Procedure Trays and Endosee System Convenience Kits contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· RECORDATI RARE DISEASES INC.

Recalled Item: Caphosol Artificial Saliva (32 doses sachet box). 64 x 15 Recalled by...

The Issue: Out of specification stability test result for the Caphosol B solution from...

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

Class II — Potential Health HazardOngoing
FoodJune 10, 2025· Yerba Prima Inc

Recalled Item: Great Plains Bentonite + Herbal Detox Capsules 60 capsules Recalled by Yerba...

The Issue: Potential contamination with Pseudomonas aeruginosa.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugJune 10, 2025· IMMUNOCORE, LLC

Recalled Item: KIMMTRAK (tebentafusp-tebn) Injection Recalled by IMMUNOCORE, LLC Due to...

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 10, 2025· Boston Foundation For Sight

Recalled Item: BostonSight SCLERAL Lens Recalled by Boston Foundation For Sight Due to...

The Issue: Select orders of lenses were manufactured with errors impacting sagittal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Foundation For Sight

Recalled Item: BostonSight PROSE Lens. Recalled by Boston Foundation For Sight Due to...

The Issue: Select orders of lenses were manufactured with errors impacting sagittal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry...

The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry...

The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products CHE Slides Recalled by Ortho-Clinical Diagnostics,...

The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products CHE Slides (Japan) Recalled by Ortho-Clinical...

The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...

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

Class II — Potential Health HazardOngoing