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. 2,727 recalls have been distributed to Maryland in the last 12 months.
Showing 17301–17320 of 52,535 recalls
Recalled Item: Protek Solo Venous Dilator Set: dilator Recalled by Cardiac Assist, Inc Due...
The Issue: On 02/26/2021, it was found that there were incorrectly packaged Dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chromosome X Alpha-Satellite in FITC Spectrum - Product Usage: Analyte...
The Issue: Users may observe additional locus specific signals at 9q34. The device pack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectrum IQ - Infusion Pump - Product Usage: intended to Recalled by Baxter...
The Issue: Potentially defective component in the AC power adapter which may fail over...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sp-4 Recalled by Washington Homeopathic Products, Inc. Due to An error...
The Issue: An error occurred where the product was manufactured with Potassium Chloride...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LCL-2-0191 Recalled by Washington Homeopathic Products, Inc. Due to An error...
The Issue: An error occurred where the product was manufactured with Potassium Chloride...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Macula Pellets Homeopathic Medicine Recalled by Washington Homeopathic...
The Issue: An error occurred where the product was manufactured with Potassium Chloride...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gentueri Viral Transport Medium (VTM) Recalled by Gentueri Inc Due to Medium...
The Issue: Medium showed visual turbidity and discoloration, potentially contaminating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaBplus and AquaBplus B2 Water Purification System - Product Usage:...
The Issue: AquaBplus HF module on the AquaBplus 2500 osmosis system, an error in the US...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dental pins - TMS LINK PLUS Self-Threading Pins - Product Recalled by...
The Issue: The incorrect dental pins were packaged and subsequently distributed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIGENE Processor SP - Product Usage: intended for processing and Recalled...
The Issue: Potential for a false-negative result for Vibrio parahaemolyticus,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Telmisartan Tablets Recalled by Alembic Pharmaceuticals Limited Due to...
The Issue: Labeling: Label-mixup
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Real Alkalized Water Recalled by Real Water, Inc. Due to FDA was notified of...
The Issue: FDA was notified of cases of acute liver failure after consumption of Real Water
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Real Alkalized Water Recalled by Real Water, Inc. Due to FDA was notified of...
The Issue: FDA was notified of cases of acute liver failure after consumption of Real Water
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sight OLO-E1/U1 Software and Operators Manual Software v2.56.1 Catalog #:...
The Issue: Discrepancy in labeling between the adult CBC ranges presented in the OLO...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinity Biotech Captia Measles IgM Kit Recalled by Clark Laboratories, Inc....
The Issue: Positive Control may run high out of its assigned ISR range and result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology...
The Issue: The shelf box identifies a small device actually contains a large device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology...
The Issue: The shelf box identifies a small device actually contains a large device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Martin-Lewis Agar Recalled by Becton Dickinson & Co. Due to Products...
The Issue: Products show heavy growth of C. albicans after 24 hours of incubation due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Martin-Lewis Agar 20 Ea - Product Usage: use Recalled by Becton...
The Issue: Products show heavy growth of C. albicans after 24 hours of incubation due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN HAKIM BACTISEAL Shunt System Clear with Barium Stripe Peritoneal...
The Issue: Incorrect labeling, Catheter did not have the required holes and markings
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.