All recall categories

Recalls distributed in Maryland

These notices name Maryland in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

4,005 stored notices name Maryland, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Maryland too — those are in the archive.

Medical devices

Reported May 10, 2023

SafeLight Fiber Optic Cable: Clear, 5MM X 10FT 3.05M, REF: 0233-050-100; Gray, 5MM X 10FT 3.05M, REF: 0233-050-200

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Corporation

FDA (openFDA device enforcement)

Medical devices

Reported May 3, 2023

(1) Carefusion V. Mueller Graves Vaginal Speculum, Catalog #GL11, Medium Blade, 4 x 1 3/8" (10.2 X 3.5cm); and (2)…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Carefusion 2200 Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 26, 2023

Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff, and Cuffless: Disposable Inner Cannula or Reusable Inner…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Covidien

FDA (openFDA device enforcement)

Medical devices

Reported Apr 26, 2023

AQURE REF 933-599 Software Versions 2.5.2 2.5.3 2.5.4 2.6.0 2.6.1 The AQURE system is intended to let you manage…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Radiometer Medical ApS

FDA (openFDA device enforcement)

Medical devices

Reported Apr 26, 2023

JOURNEY II UNI XLPE TIBIA INSERT MEDIAL SZ 7-8 8MM

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Smith & Nephew, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 19, 2023

Zone Perfect Fudge Graham bar 50g bars packaged in foil wrapped- 12 bars individually wrapped per cardboard carton

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Laboratories

FDA (openFDA food enforcement)

Medical devices

Reported Apr 19, 2023

Edward Lifesciences, REF 777F8, Swan-Ganz CCOmbo V, CCO/SvO2/CEDV/VIP, Thermodilution Catheter, Exterior Diameter 8F…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Edwards Lifesciences, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 19, 2023

EMPOWR Porous Knee Patella Over Drill, REF: 802-05-104; EMPOWR Knee Patella Drill, REF: 802-05-108

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Encore Medical, LP

FDA (openFDA device enforcement)

Medical devices

Reported Apr 19, 2023

Flex-Neck Catheter External Repair Kit REF CE-1400 LOT CE-1400/A

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Merit Medical Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 19, 2023

Frozen Organic Strawberries, Kirkland Signature, frozen, net wt. 4lb., 9 packages per case, Costco Item 904984. UPC…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Scenic Fruit Company, LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 19, 2023

thermage THERMAGE CPT SYSTEM REF TG-2B *** Solta Medical, Inc. thermage RF GENERATOR REF TG-2B *** Solta Medical, Inc.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Solta Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 19, 2023

Digital VIPR ROC-9839 Roberts Oxygen Ready to Use Digital VIPR (head only) ROC-9840, Roberts Oxygen Ready to Use…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Western/Scott Fetzer Company

FDA (openFDA device enforcement)

Medical devices

Reported Apr 12, 2023

Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath, 8.5F(Small), REF D-1385-01-S, RX CE 2797, Sterile

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biosense Webster, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 12, 2023

Astor Chocolate Wafer Stick NWT WT. 11.64 OZ 330g UPC 72375102886

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Eastland Food Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Apr 12, 2023

Tempus Pro Patient Monitor is a portable vital signs monitor intended to be used by clinicians and medically qualified…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 5, 2023

COVIDIEN Shiley Lo-Pro Oral/Nasal Tracheal Tube Cuffed REF 86051 7.0 mm I.D. The Shiley Lo-Pro Oral/Nasal Tracheal Tube…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Covidien

FDA (openFDA device enforcement)

Medical devices

Reported Apr 5, 2023

Instructions for Use for the following Leksell Stereotactic System and Leksell Neurosurgical Instruments: (1) Part…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Elekta Instrument AB

FDA (openFDA device enforcement)

Medical devices

Reported Apr 5, 2023

Irvine Scientific Oil for Embryo Culture (Light Mineral Oil) REF Catalog # 9305

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Fujifilm Irvine Scientific, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 5, 2023

Color Cuff Single Port, Single Bladder 30 (Royal Blue) Quick Connect, REF: 5921-030-135; Color Cuff Dual Port, Single…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Food

Reported Apr 5, 2023

ISH Shrimpish Sample Meal Kit: ( Sample Meal Kit ) a package containing two ISH Foods plant-based Shrimpish products…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

The Ish Company

FDA (openFDA food enforcement)

Food

Reported Mar 29, 2023

Kirkland Signature Colombian Cold Brew Coffee ready-to-drink, 12 fl oz in aluminum can, 12 cans per case

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Berner Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 29, 2023

BD Pyxis Anesthesia ES System (PAS ES), REF: 327; BP Pyxis MedStation ES (Med ES Main), REF: 323; BD Pyxis MedStation…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 29, 2023

DG Health brand Sugar Free Daily Fiber in 10 oz. plastic containers (UPC: 860005934294).

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Dollar General Corporation

FDA (openFDA food enforcement)

Meat & poultry

Reported Mar 24, 2023

Elkhorn Valley Packing Recalls Boneless Beef Chuck Product Due to Possible E. coli O103 Contamination

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Elkhorn Valley Packing LLC

USDA FSIS

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Other states

RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.