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.
Showing 24481–24500 of 52,535 recalls
Recalled Item: Heparin 10 mL/Marcain 0.25% 20 mL/Sodium Bicarbonate 8.4%-40 mL/per 70 mL...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin 2 mL/Lidocaine 2%-10 mL/Sodium Bicarbonate 8.4%-5mL/ Sterile Water...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HCG 4 Recalled by Anderson Compounding Pharmacy, Inc. DBA Anderson...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Streptomycin 24 mg/Dexamethasone 10 mg/mL Otic Injection Recalled by...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin 20 Recalled by Anderson Compounding Pharmacy, Inc. DBA Anderson...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexamethasone 24 mg/mL Injection Recalled by Anderson Compounding Pharmacy,...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gentamicin 160 mg/1000 mL Sterile Water for Irrigation Recalled by Anderson...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mobi-C 14mm Distraction Screw Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Incorrect part description contained on an additional label placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dornier Diode Laser Fibers:Used with Dornier Medilas D Family Lasers...
The Issue: Pin hole package failures compromising sterility of product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus MAJ-209 Single Use Suction Valves Recalled by Olympus Corporation of...
The Issue: There is a potential for the single use suction valve to come apart and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci SP surgical system Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Intuitive has become aware that the da Vinci SP system may trigger a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlideScope Video Laryngoscope Recalled by Verathon, Inc. Due to A...
The Issue: A typographical error in the Operations & Maintenance Manual incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Flowable Wound Matrix Catalog No: FWD301 Product Usage: Integra...
The Issue: Stability did not meet acceptance criteria for visual appearance during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breads from Anna Black Bean Brownie Mix 14oz Recalled by Wholesome Treats,...
The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Breads from Anna Dairy & Corn Free Bread Mix 19oz Recalled by Wholesome...
The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...
Recommended Action: Do not consume. Return to store for a refund or discard.