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. 2,636 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,636 in last 12 months

Showing 3506135080 of 52,535 recalls

DrugAugust 2, 2016· Actavis Inc

Recalled Item: Hydrocortisone and acetic acid otic solution Recalled by Actavis Inc Due to...

The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 2, 2016· Hologic, Inc

Recalled Item: SureSight Obturator Introducer Localization Systems (ILS) for ATEC in MRI....

The Issue: Tip Breakage at the glue joint between the obturator body and tip

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Alere San Diego, Inc.

Recalled Item: LDX Optical Check Cassettes (OCC) Model Number: 10-228 and 14-535 Recalled...

The Issue: Incorrect expiration date on the magnetic strip that does not match the...

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

Class III — Low RiskOngoing
Medical DeviceAugust 2, 2016· Randox Laboratories Ltd.

Recalled Item: Randox Lipase (Colorimetric) Product Usage: A lipase test system is Recalled...

The Issue: According to the firm carry over was observed when the Lipase test is run...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Zimmer Biomet, Inc.

Recalled Item: Uniflex Humeral Nail: 467265 G-PIN 2.8BL 3.2PL 60CM 2PK Pin Recalled by...

The Issue: The G-PIN 2.8BL 3.2PL 60 CM 2PK is intended to contain one (1) 467265-01...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Bayer Healthcare

Recalled Item: Certegra Workstation used in conjunction with Medrad Stellant CT Injection...

The Issue: CertegraWorkstation when used in conjunction with the Medrad Stellant CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo Plaza picture archiving and communication system (PAC) (PACS) intended...

The Issue: Siemens is releasing a Customer Advisory Notice to explain meaning of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Becton Dickinson & Company

Recalled Item: catalog # 405612 BD Spinal Anesthesia Tray 22G x 3.5 Recalled by Becton...

The Issue: A recall was initiated by Hospira, Inc. for several lots of 5% Lidocaine HCI...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Hologic, Inc

Recalled Item: SureSight Obturator Introducer Localization Systems (ILS) for ATEC in MRI....

The Issue: Tip Breakage at the glue joint between the obturator body and tip

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.Plaza VB 10 A Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens is releasing a Customer Advisory Notice to explain meaning of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Multix Fusion VA10 Product Usage: The Multix Fusion VA10 system Recalled by...

The Issue: Siemens became aware of a potential issue with the patient table for Ysio...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2016· Ethicon, Inc.

Recalled Item: ETHICON MERSILENE" Tape (also to as MERSILENETM Polyester Fiber Recalled by...

The Issue: ETHICON MERSILENE" Tape (also to as MERSILENETM Polyester Fiber Strip or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Patella Assembly Instrument Recalled by Stryker...

The Issue: Upon failure of the press-fit, the clamping sub components and pins could...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Multix Fusion Stationary X-Ray System Product Usage: The Multix Fusion...

The Issue: Siemens became aware of a potential issue with the patient table for Ysio...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: YSIO Max Product Usage: The Ysio Max is a radiographic Recalled by Siemens...

The Issue: Siemens became aware of a potential issue with the patient table for Ysio...

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

Class II — Potential Health HazardOngoing
DrugAugust 1, 2016· Isomeric Pharmacy Solution, LLC

Recalled Item: Betamethasone Acetate / Betamethasone Sodium Phosphate Injectable Suspension...

The Issue: Lack of processing controls: Isomeric Pharmacy Solution, LLC is recalling...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 1, 2016· Life Rising Corp S

Recalled Item: The product is packaged in a white plastic bottle with Recalled by Life...

The Issue: The dietary supplement contains lead.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 29, 2016· Drews LLC

Recalled Item: SimplyNature Organic Chipotle Ranch Dressing Recalled by Drews LLC Due to...

The Issue: Product contains undeclared wheat.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 29, 2016· Hampton Creek Foods

Recalled Item: JUST Cinnamon Roll Coffee Cake Mix Recalled by Hampton Creek Foods Due to...

The Issue: Firm received a positive test result for Salmonella in Coconut Milk powder...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 29, 2016· Hampton Creek Foods

Recalled Item: JUST White Cake Mix Recalled by Hampton Creek Foods Due to Potential...

The Issue: Firm received a positive test result for Salmonella in Coconut Milk powder...

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

Class I — Serious Health HazardOngoing
Refund