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. 2,674 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,674 in last 12 months

Showing 2756127580 of 52,535 recalls

Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
DrugJune 8, 2018· Qualgen, LLC

Recalled Item: TESTOSTERONE 200 mg PELLET Recalled by Qualgen, LLC Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date.

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

Class III — Low RiskOngoing
Refund
DrugJune 8, 2018· Ingenus Pharmaceuticals Llc

Recalled Item: Irinotecan Hydrochloride Injection Recalled by Ingenus Pharmaceuticals Llc...

The Issue: Superpotent Drug: High out of specification assay value results for potency.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2018· Qualgen, LLC

Recalled Item: ESTRADIOL 20mg PELLET Recalled by Qualgen, LLC Due to Labeling: Incorrect or...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date.

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

Class III — Low RiskOngoing
Refund
DrugJune 8, 2018· Ingenus Pharmaceuticals Llc

Recalled Item: Irinotecan Hydrochloride Injection Recalled by Ingenus Pharmaceuticals Llc...

The Issue: Superpotent Drug: High out of specification assay value results for potency.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 7, 2018· GE Medical Systems, LLC

Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...

The Issue: The latest on-site software version may not have been reinstalled at some...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2018· GE Medical Systems, LLC

Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...

The Issue: The latest on-site software version may not have been reinstalled at some...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2018· GE Medical Systems, LLC

Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...

The Issue: The latest on-site software version may not have been reinstalled at some...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2018· GE Medical Systems, LLC

Recalled Item: Discovery MR750w Nuclear Magnetic Resonance Imaging System labeled as the...

The Issue: GE Medical Systems has discovered a small area on the bore surface of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Single Chamber Temporary External Pacemaker Recalled by Medtronic Inc.,...

The Issue: A subset of Medtronic Model 53401 Single Chamber External Pulse Generators...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2018· Tosoh Bioscience Inc

Recalled Item: G8 Automated HPLC Analyzer: HLC-723G8-ST Recalled by Tosoh Bioscience Inc...

The Issue: HbAE is known to interfere with the HbA1c assay on the current version of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2018· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...

The Issue: The firm has learned that some RayStation/RayPlan users have commissioned...

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

Class II — Potential Health HazardOngoing
DrugJune 6, 2018· Pharmalucence, Inc.

Recalled Item: Kit for the Preparation of Technetium Tc99m Medronate Recalled by...

The Issue: Lack of assurance of sterility: Technetium TC-99M Medronate Kit has a...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2018· PharMEDium Services, LLC

Recalled Item: HYDROmorphone HCl 0.5 mg per mL in 0.9% Sodium Chloride Recalled by...

The Issue: Superpotent and Subpotent

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 4, 2018· HOSPIRA INC, LAKE FOREST

Recalled Item: Naloxone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST Due to...

The Issue: Presence of Particulate Matter; Potential for particulate matter on the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 4, 2018· B. Braun Medical, Inc.

Recalled Item: 26-Lead Transfer Set for use with APEX¿ Compounding System Recalled by B....

The Issue: There is a potential for valves on the 26-Lead Transfer Set to be...

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

Class II — Potential Health HazardOngoing