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. 2,787 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,787 in last 12 months

Showing 1626116280 of 29,093 recalls

Medical DeviceMay 18, 2018· OMNIlife science Inc.

Recalled Item: OMNI Hip System Recalled by OMNIlife science Inc. Due to The Internal...

The Issue: The Internal packaging, the pouch and patient labels are improperly labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2018· Natus Neurology DBA Excel Tech., Ltd. (XLTEK)

Recalled Item: Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Recalled...

The Issue: Natus Neuro has discovered a possible manufacturing defect in the ErgoJust...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2018· Qiagen Sciences, Inc.

Recalled Item: AmniSure ROM Test under the following labels: 1) Catalog Number Recalled by...

The Issue: Potential for control line not appearing on the test strip

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2018· Arrow International Inc

Recalled Item: VPS TipTracker Stylet Accessory Recalled by Arrow International Inc Due to...

The Issue: Product pouch label may not easily identify the lot number, expiration date...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2018· Arrow International Inc

Recalled Item: VPS Rhythm ECG Accessory Pack Recalled by Arrow International Inc Due to...

The Issue: Product pouch label may not easily identify the lot number, expiration date...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2018· Arrow International Inc

Recalled Item: VPS Rhythm ECG Accessory Pack with Johans Adapter Recalled by Arrow...

The Issue: Product pouch label may not easily identify the lot number, expiration date...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2018· Arrow International Inc

Recalled Item: Peripherally Inserted Midline Catheter Kit with Placement Wire Recalled by...

The Issue: Product pouch label may not easily identify the lot number, expiration date...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: BEAD TIP GD WIRE 3.0MM X 60CM Recalled by Zimmer Biomet, Inc. Due to The...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: The Recalled by Abbott Laboratories, Inc Due to An update to the Reagents...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: C3 is an in vitro diagnostic assay for the quantitative Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: Transferrin is an in vitro diagnostic assay for the quantitative Recalled by...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: Apolipoprotein B is an in vitro diagnostic assay for the Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: Immunoglobulin G is an in vitro diagnostic assay for the Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: Immunoglobulin A is an in vitro diagnostic assay for the Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: Apolipoprotein A1 is an in vitro diagnostic assay for the Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: Immunoglobulin M is an in vitro diagnostic assay for the Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Elekta, Inc.

Recalled Item: HexaPOD evo RT Couch Top (also known as HexaPOD evo Module) Recalled by...

The Issue: Upon completion of a 6D workflow, the HexaPOD evo Module may be in a tilted...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: C4 is an in vitro diagnostic assay for the quantitative Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Ion Beam Applications S.A.

Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to Correction vector...

The Issue: Correction vector confirmation message is lost if access point is changed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: G-PIN 2.8BL 3.2PL 98CM 2PK Recalled by Zimmer Biomet, Inc. Due to The firm...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing