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. 2,871 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,871 in last 12 months

Showing 62216240 of 52,535 recalls

Medical DeviceApril 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE LUER LOCK DISPOSABLE SYRINGE WITHOUT NEEDLE Recalled by MEDLINE...

The Issue: It has been identified that testing documentation does not support that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2024· Alcon Research LLC

Recalled Item: ClearCut S Safety Sideport Knife 1.2mm Dual Bevel Model/Catalog Number:...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2024· Alcon Research LLC

Recalled Item: 20 Gauge V-Lance Knife Model/Catalog Number: 8065912001 Software Version:...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2024· Alcon Research LLC

Recalled Item: ClearCut S Safety Sideport Knife 1.0mm Dual Bevel Model/Catalog Number:...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2024· Mirion Technologies (Capintec), Inc.

Recalled Item: Captus 4000e Thyroid Uptake System. Intended to be used to Recalled by...

The Issue: Complaints of unexpected detachment of the collimator have been reported.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2024· Mirion Technologies (Capintec), Inc.

Recalled Item: Captus 4000e Thyroid Uptake System with Well. Intended to be Recalled by...

The Issue: Complaints of unexpected detachment of the collimator have been reported.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2024· Mirion Technologies (Capintec), Inc.

Recalled Item: Captus 4000e Thyroid Uptake System with Well and 2 inch Recalled by Mirion...

The Issue: Complaints of unexpected detachment of the collimator have been reported.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2024· Alcon Research LLC

Recalled Item: ClearCut Sideport Knife Dual Bevel 1.2mm Angled Model/Catalog Number:...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2024· Philips North America Llc

Recalled Item: Ingenia 1.5T with Evolution Upgrade 1.5T - Magnetic Resonance (MR) Recalled...

The Issue: Philips Ingenia Evolution systems with software R5.7.1 may not provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2024· Philips North America Llc

Recalled Item: Ingenia 3.0T with Evolution Upgrade 3.0T - - Magnetic Resonance Recalled by...

The Issue: Philips Ingenia Evolution systems with software R5.7.1 may not provide...

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

Class II — Potential Health HazardOngoing
DrugApril 20, 2024· Revive Rx LLC dba Revive Rx Pharmacy

Recalled Item: Tirzepatide 10 mg/0.5 mL Sterile Solution Recalled by Revive Rx LLC dba...

The Issue: Labeling: Label Mix-up - product labeled as tirzepatide contains...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 19, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Amphotericin B Liposome for Injection Recalled by SUN PHARMACEUTICAL...

The Issue: Out of specification for assay

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 19, 2024· Nomax Inc

Recalled Item: GloStrips Recalled by Nomax Inc Due to Failed Impurities/Degradation...

The Issue: Failed Impurities/Degradation Specifications: The Active Pharmaceutical...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 19, 2024· Nomax Inc

Recalled Item: FUL-GLO Recalled by Nomax Inc Due to Failed Impurities/Degradation...

The Issue: Failed Impurities/Degradation Specifications: The Active Pharmaceutical...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 19, 2024· Nomax Inc

Recalled Item: GloStrips Recalled by Nomax Inc Due to Failed Impurities/Degradation...

The Issue: Failed Impurities/Degradation Specifications: The Active Pharmaceutical...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 19, 2024· Nomax Inc

Recalled Item: FUL-GLO Recalled by Nomax Inc Due to Failed Impurities/Degradation...

The Issue: Failed Impurities/Degradation Specifications: The Active Pharmaceutical...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 19, 2024· Philips North America Llc

Recalled Item: Patient Information Center iX and Patient Information Center iX Expand...

The Issue: Event Catalog information does not save when copied and transferred from one...

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

Class II — Potential Health HazardOngoing
FoodApril 18, 2024· Graceleigh, Inc. dba Sammy's Milk

Recalled Item: Sammy's Milk GOAT MILK TODDLER FORMULA Recalled by Graceleigh, Inc. dba...

The Issue: FDA inspection and investigation of firm's website and social media pages...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 18, 2024· Graceleigh, Inc. dba Sammy's Milk

Recalled Item: Sammy's Milk GOAT MILK TODDLER FORMULA Recalled by Graceleigh, Inc. dba...

The Issue: FDA inspection and investigation of firm's website and social media pages...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 18, 2024· Stryker Neurovascular

Recalled Item: The Synchro2 Guidewires are a steerable guidewire family with a Recalled by...

The Issue: Stryker Neurovascular has observed an increased frequency of PTFE coating...

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

Class II — Potential Health HazardOngoing