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. 2,858 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,858 in last 12 months

Showing 70417060 of 52,535 recalls

Medical DeviceJanuary 29, 2024· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Embrace Drill Tower Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due...

The Issue: The surgical techniques for the Embrace Shoulder Instruments -Drill Tower...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2024· Canon Medical System, USA, INC.

Recalled Item: MRI system: Vantage Orian Recalled by Canon Medical System, USA, INC. Due to...

The Issue: For some MRI systems, it has been found that some of the maximum Spatial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2024· NxStage MDS Corporation

Recalled Item: NxStage Cartridge Express with Speedswap Recalled by NxStage MDS Corporation...

The Issue: Product is recalled due to reports of blood leaking or spraying from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2024· In2Bones, SAS

Recalled Item: I.B.S¿ 6.5-C Compression screw - diam 6.5mm lg 80mm Recalled by In2Bones,...

The Issue: This Field Action is being conducted following the identification of a batch...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2024· In2Bones, SAS

Recalled Item: I.B.S¿ 6.5-C Compression screw - diam 6.5mm lg 75mm Recalled by In2Bones,...

The Issue: This Field Action is being conducted following the identification of a batch...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS 5600 Integrated System Catalog Nos. 6802413 (regular) and 6802915...

The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics,...

The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS XT 3400 Chemistry System Recalled by Ortho-Clinical Diagnostics, Inc....

The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics,...

The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS 3600 Immunodiagnostic System Catalog Nos. 6802783 (regular) and...

The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS 4600 Chemistry System Catalog Nos. 6802445 (regular) and 6900440...

The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS 5600 Integrated System Catalog Nos. 6802413 (regular) and 6802915...

The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS 4600 Chemistry System Catalog Nos. 6802445 (regular) and 6900440...

The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS 3600 Immunodiagnostic System Catalog Nos. 6802783 (regular) and...

The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS XT 3400 Chemistry System Recalled by Ortho-Clinical Diagnostics, Inc....

The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2024· Alphatec Spine, Inc.

Recalled Item: IdentiTi ALIF Standalone Interbody System: Part Number/Description...

The Issue: Due to reports of intraoperative graft bolt implantation breakages.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2024· BioFire Diagnostics, LLC

Recalled Item: FilmArray Gastrointestinal (GI) Panel RFIT-ASY-0116 (30 test kit)...

The Issue: Due to potential signals of increased false positive Norovirus results when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2024· BioFire Diagnostics, LLC

Recalled Item: BIOFIRE Blood Culture Identification 2 (BCID2) Panel when used with:...

The Issue: Due to a trend in false positive Candida tropicalis results on blood culture...

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

Class II — Potential Health HazardOngoing
FoodJanuary 25, 2024· Lidl US TRADING

Recalled Item: Banana Pepper Rings 16 FL OZ (1PT) 473ml . Packaged Recalled by Lidl US...

The Issue: Container integrity issued (punctured lid)

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

Class III — Low RiskOngoing
Refund
FoodJanuary 25, 2024· MG Foods Middletown

Recalled Item: Authentic Fresh to You Deluxe Triple Decker Club Net Wt. Recalled by MG...

The Issue: Undeclared egg

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

Class I — Serious Health HazardOngoing
Refund