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 2440124420 of 52,535 recalls

DrugApril 8, 2019· Customceutical Compounding

Recalled Item: BPlex (METHYLCOBALAMIN 1000 MCG/ML PYRIDOXAL 5 PHOSPHATE 20MG/ML...

The Issue: Lack of assurance of sterility for injectables and solutions intended to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 8, 2019· Customceutical Compounding

Recalled Item: Lipoplex (METHIONINE 25 MG/ML INOSITOL 50 MG/ML CHOLINE CHLORIDE 50 Recalled...

The Issue: Lack of assurance of sterility for injectables and solutions intended to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 8, 2019· Customceutical Compounding

Recalled Item: Test D (TESTOSTERONE CYPIONATE 200MG/ML VITAMIN D3 5 Recalled by...

The Issue: Lack of assurance of sterility for injectables and solutions intended to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 8, 2019· Customceutical Compounding

Recalled Item: BPlex (METHYLCOBALAMIN 1000 MCG/ML PYRIDOXAL 5 PHOSPHATE 20MG/ML...

The Issue: Lack of assurance of sterility for injectables and solutions intended to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 8, 2019· Customceutical Compounding

Recalled Item: Trimix HIGH (Papaverine HCl 30 mg/mL Phentolamine Mesylate 2 mg/mL Recalled...

The Issue: Lack of assurance of sterility for injectables and solutions intended to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 8, 2019· Customceutical Compounding

Recalled Item: HCG (CHORIONIC GONADOTROPIN 1000 IU/ML PEP 25 mg/mL) inj 5 Recalled by...

The Issue: Lack of assurance of sterility for injectables and solutions intended to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2019· Brian P. Richardson

Recalled Item: Kopi Jantan Tradisional Natural Herbs Coffee Recalled by Brian P. Richardson...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to be...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 5, 2019· Abbott Gmbh & Co. KG

Recalled Item: Alinity i Processing Module Recalled by Abbott Gmbh & Co. KG Due to...

The Issue: Potential loose cable connections on the reagent cooler, which could result...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2019· Roche Diagnostics Corporation

Recalled Item: cobas p 501 post-analytical units Recalled by Roche Diagnostics Corporation...

The Issue: There is a potential for the tray input flap on the post analytical units to...

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

Class III — Low RiskOngoing
Medical DeviceApril 4, 2019· Roche Diagnostics Corporation

Recalled Item: cobas p 701 post-analytical units Recalled by Roche Diagnostics Corporation...

The Issue: There is a potential for the tray input flap on the post analytical units to...

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

Class III — Low RiskOngoing
Medical DeviceApril 4, 2019· Advanced Bionics, LLC

Recalled Item: SoundWave Professional Suite Software 3.2 Recalled by Advanced Bionics, LLC...

The Issue: The manufacturer received complaints that customers were attempting to...

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

Class III — Low RiskOngoing
Medical DeviceApril 3, 2019· Bio-Rad Labs

Recalled Item: Autoimmune EIA Anti-Tissue Transglutaminase (tTG) IgA Test Recalled by...

The Issue: An elevated lot-to-lot bias was observed for Autoimmune EIA Anti-Tissue...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2019· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: 2008T BlueStar Machine Software v.2.72-Hemodialysis machine Model Number:...

The Issue: Power Logic Board Fail Message on the 2008T BlueStar Machine with software...

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

Class III — Low RiskOngoing
Medical DeviceApril 3, 2019· Becton Dickinson & Co.

Recalled Item: BD Veritor System Reader -In Vitro Diagnostic for use with Recalled by...

The Issue: Background calibration has the potential to cause false positive or false...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2019· Becton Dickinson & Co.

Recalled Item: BD Veritor Plus Analyzer- In-Vitro Diagnostic intended to use with Recalled...

The Issue: Background calibration has the potential to cause false positive or false...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2019· Thommen Medical AG

Recalled Item: Adapter for handpiece Recalled by Thommen Medical AG Due to Dental adaptor...

The Issue: Dental adaptor does not conform to specifications. The dental coupling of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2019· Elekta Limited

Recalled Item: Elekta Unity systems Product Usage: Elekta Unity using Magnetic Resonance...

The Issue: There is no warning in the Elekta Unity manual for the administration of...

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

Class II — Potential Health HazardOngoing
FoodApril 3, 2019· ConAgra Foods, INc.

Recalled Item: Hunts Tomato Paste No Salt Added 6 ounce cans Recalled by ConAgra Foods,...

The Issue: Mold. This situation is due to potential damage to the cans.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Estrone 5mg/mL Oil Injection Recalled by Anderson Compounding Pharmacy, Inc....

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Prostaglandin Tri-Mix 50:30:1 Recalled by Anderson Compounding Pharmacy,...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund