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. 2,774 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,774 in last 12 months

Showing 1868118700 of 29,093 recalls

Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N363) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-GN82) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N315) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-P644) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-P621) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N217) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N292) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-P606) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-P629) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N350) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-P603) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N211) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N293) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N265) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Acumed LLC

Recalled Item: The Acumed Slide-Loc Anatomic Radial Head System is intended for Recalled by...

The Issue: The firm initiates a voluntary removal and discontinue marketing of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2017· Ortho Solutions Inc

Recalled Item: Oxford/Oxbridge AFN End Cap 10 mm x 5 mm tp Recalled by Ortho Solutions Inc...

The Issue: There is a material mislabeling of the AFN End Cap.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2017· Olympus Corporation of the Americas

Recalled Item: High Frequency Resection Electrodes Recalled by Olympus Corporation of the...

The Issue: Loop wires breaking at the distal end of the Monopolar HF Resection Electrodes.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2017· Abbott Laboratories

Recalled Item: ARCHITECT SHBG Reagent The ARCHITECT SHBG assay is a chemiluminescent...

The Issue: Firm has identified that ARCHITECT SHBG results generated with the Potassium...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2017· Zimmer Biomet, Inc.

Recalled Item: AFFIXUS Hip Fracture Nail Product Usage: The Hip Fracture Nail Recalled by...

The Issue: nail not properly engaging with the targeting jig due to certain undersized...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2017· ConMed Corporation

Recalled Item: Nonabsorbable suture anchor system intended to reattach soft tissue to...

The Issue: Manufactured with the incorrect anchor outer body

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

Class II — Potential Health HazardOngoing