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. 2,782 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,782 in last 12 months

Showing 1738117400 of 29,093 recalls

Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: rHead Stem Implant 6mm Collar Recalled by Howmedica Osteonics Corp. Due to...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: #1 Bipolar stem implant (Sterile packed). Orthopedic implant for replacement...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2017· Medline Industries Inc

Recalled Item: Sensicare Green Surgical Glove Recalled by Medline Industries Inc Due to...

The Issue: Possible open seal on top portion of the package. Could cause breach of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2017· Terumo BCT, Inc.

Recalled Item: HARVEST TERUMOBCT Recalled by Terumo BCT, Inc. Due to Certain lots of the...

The Issue: Certain lots of the Harvest Graft Delivery System GDP-10 Procedure Packs may...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Cook Inc.

Recalled Item: Mallinckrodt Institute Percutaneous Gastrostomy Set Product Usage: Intended...

The Issue: Cook has identified that the affected lots may contain wire guides that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR Recalled by Johnson &...

The Issue: Some contact lenses were associated with complaints of a foreign matter...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE OASYS Brand Contact Lenses with HYDRACLEAR PLUS Recalled by Johnson &...

The Issue: Some contact lenses were associated with complaints of a foreign matter...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Johnson & Johnson Vision Care, Inc.

Recalled Item: 1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses Recalled by Johnson...

The Issue: Some contact lenses were associated with complaints of a foreign matter...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Cook Inc.

Recalled Item: Wills-Oglesby Percutaneous Gastrostomy Set Product Usage: Intended for the...

The Issue: Cook has identified that the affected lots may contain wire guides that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Cook Inc.

Recalled Item: Percutaneous Gastrojejunostomy Set Product Usage: Intended for the...

The Issue: Cook has identified that the affected lots may contain wire guides that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2017· Teleflex Medical

Recalled Item: Teleflex(R) Percuvance(TM) Percutaneous Surgical System Recalled by Teleflex...

The Issue: Teleflex is recalling these products because the jaws of the tool tip may...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2017· BioMerieux SA

Recalled Item: NucliSENS Lysis Buffer Extended lot for RES 76675 Recalled by BioMerieux SA...

The Issue: Elute may become colored due to the residual presence of heme group...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Multi Lumen Central Venous Catheterization Kit Recalled by Arrow...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue Two Lumen Hemodialysis Catheterization Kit for High Volume...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue Plus Multi Lumen CVC (Central venous catheter) Recalled by...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi Lumen Central Venous Catheterization Kit with Blue...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Central Venous Catheterization Kit with Blue FlexTip Catheter Recalled by...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing