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. 1,928 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
1,928 in last 12 months

Showing 2082120840 of 52,535 recalls

DrugJanuary 14, 2020· Pharmaceutical Associates Inc

Recalled Item: Nystatin Oral Suspension Recalled by Pharmaceutical Associates Inc Due to...

The Issue: Subpotent: Out of specification for assay at the 12-month time point.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 14, 2020· Hikma Pharmaceuticals USA Inc.

Recalled Item: methylPREDNISolone Sodium Succinate For Injection Recalled by Hikma...

The Issue: Labeling: Incorrect Instructions: Vial label incorrectly instructs...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 13, 2020· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Telescopic Uncoated (Push Button) Recalled by Stryker Instruments Div. of...

The Issue: Hairline fractures in a component could allow electrical current to arc out...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2020· Philips North America, LLC

Recalled Item: Philips DigiTrak XT Holter Recorder Software version number B.1 and Recalled...

The Issue: if an AAA battery is inserted in the recorder and a user attempts to start...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2020· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: DP-30 Digital Ultrasonic Diagnostic Imaging System Recalled by Mindray DS...

The Issue: The DP-30 displays an incorrect needle-guide bracket when used with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2020· CooperVision Inc.

Recalled Item: Coopervision Vertex Toric /2 Clear Toric- Power -2.50 -0.75 /90 Recalled by...

The Issue: Incorrect power of lenses than the expected

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2020· C.R. Bard Inc

Recalled Item: The Bard Intra-abdominal Pressure Monitoring Device is composed of a...

The Issue: Leaks or disconnect near the sampling port of the Intra Abdominal Pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2020· CooperVision Inc.

Recalled Item: Coopervision Vertex Toric /2 Clear Toric- Power +2.25 -0.75/120 Soft...

The Issue: Incorrect power of lenses than the expected

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2020· Stryker Instruments Div. of Stryker Corporation

Recalled Item: SafeAir Telescopic Smoke Evacuation Pencil Recalled by Stryker Instruments...

The Issue: Hairline fractures in a component could allow electrical current to arc out...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2020· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Telescopic Smoke Evac Pencil Recalled by Stryker Instruments Div. of Stryker...

The Issue: Hairline fractures in a component could allow electrical current to arc out...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Reaction Ring Segment Recalled by Siemens Healthcare...

The Issue: Some lots ending in "17", "18", "19", or higher may have cuvette defects...

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

Class II — Potential Health HazardOngoing
FoodJanuary 12, 2020· Sugar Foods Corporation

Recalled Item: Granulate Pure Cane Sugar sold under the brand names of: Ahold 16 oz...

The Issue: They were notified by their supplier that the product may be contaminated...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 ROYALSILK SURGGOWN BNS 2XL Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 NON-RNF SURG GOWN 3XL LONG Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 FABRIC REINF SURG GOWN 2XL Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 NONREIN SURGGOWN BNS XL Recalled by Cardinal Health Due to The gowns...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 NONREINF SURG GOWN 2XL XLONG Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 FABRIC REINFORCEDGown 2XL NS Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 ROYALSILK SCRBNURGOWN BNS L Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 NON-REINF SURG GWN 3XL XLONG Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing