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.
4,061 stored notices name Maryland, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Maryland too — those are in the archive.
Reported Jun 5, 2019
Abbott MitraClip XTR Clip Delivery System, UDI: 08717648226366, Part: CDS0601-XTR, Sterile EO, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Vascular
FDA (openFDA device enforcement)
Reported Jun 5, 2019
Horizon Cardiology Hemo
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Change Healthcare Israel Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2019
Dole Classic Coleslaw (US) Shredded cabbage and carrots. 14 oz. US
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dole Fresh Vegetables
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 5, 2019
King LTS-D Kit Size 1, Model Number KLTSD431
Moderate riskThis product could cause temporary or reversible health problems — stop using it.King Systems Corp. dba Ambu, Inc.
FDA (openFDA device enforcement)
Reported Jun 5, 2019
Suja Organic Kombucha - Ginger Lemon: 15.2 oz. glass bottle; UPC 818617020232 DISTRIBUTED BY SUJA LIFE, LLC OCEANSIDE,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Suja Life LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported May 29, 2019
EV1000 Clinical Platform, Models: EV1000A, EV1000NI, EV1000CS Product Usage: EV1000A Monitor is used to optimize fluid…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported May 29, 2019
Leksell GammaPlan 11.1 Product Usage: Leksell GammaPlan is a computer-based system designed for Leksell Gamma Knife…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta Instrument AB
FDA (openFDA device enforcement)
Reported May 29, 2019
DEXIS Titanium Intraoral Sensor Product Usage: The DEXIS Titanium Intraoral Sensor is a USB-driven sensor which is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.KaVo Dental Technologies LLC
FDA (openFDA device enforcement)
Reported May 29, 2019
Thio Med w/Dex, Hem, Vit K (5ml) 100/PK Product Usage; Recommended for use in qualitative procedures as a general…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
13 more products in this recall
FDA (openFDA device enforcement)
Reported May 29, 2019
Drill Sys 2.7, 2x105mm, stryker, Item Number 502015106
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer GmbH
75 more products in this recall
FDA (openFDA device enforcement)
Reported May 22, 2019
Abbott ARCHITECT Estradiol Reagent Kit - Product Usage: The ARCHITECT Estradiol assay is a Chemiluminescent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Ireland Diagnostics Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 22, 2019
Fungitell Kit, Catalog FT001 - Product Usage: The Fungitell assay is a potease zymogen-based colorimetric assay for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Associates
FDA (openFDA device enforcement)
Reported May 22, 2019
MediPress pneumatic compression system, Half Leg-Segmental Gradient, Model #6102-S
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Compass Health Brands (Corporate Office)
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 22, 2019
Frozen ground tuna, 1 lb package, 20 packages/case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jensen Tuna Inc.
FDA (openFDA food enforcement)
Reported May 22, 2019
Pentax Medical C2 CryoBalloon Standard Focal Catheter, Model FG 1028, Sterile, RX. Product Usage: The C2 CryoBalloon…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pentax
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 22, 2019
Artis Zee (material # 10094135, 10094137, 10094141) - Product Usage: AXIOM Artis zee and Q/ Q.zen is a family of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 22, 2019
Signature Kitchens Green Peas & Diced Carrots; Net Wt 16 oz (1 lb) 453 g; UPC 2113009154; frozen
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Twin City Foods Inc.
FDA (openFDA food enforcement)
Reported May 15, 2019
Abbott ARCHITECT cSystems ICT Module, REF 09D28-03. Product Usage: The ARCHITECT cSystems ICT (Integrated Chip…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories, Inc.
FDA (openFDA device enforcement)
Reported May 15, 2019
Neuro Omega System, incorporating HaGuide software. For neurological and neurosurgical use. To monitor, record and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Alpha Omega Engineering
FDA (openFDA device enforcement)
Reported May 15, 2019
Dried whole elderberry, Oregon s Wild Harvest brand, packaged in metalized plastic bag, net wt. 4 oz or 1 lb. Each case…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oregons Wild Harvest Inc.
FDA (openFDA food enforcement)
Reported May 15, 2019
Atellica IM 1300 Analyzer, Material Number 11066001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 15, 2019
Wegmans Food You Feel Good About Cilantro Lime Green Sauce. A finishing sauce for meats, seafood & Veggies in 8 oz.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wegmans Food Markets, Inc.
FDA (openFDA food enforcement)
Reported May 15, 2019
T7 Driver Cannulated AO (Part Number 110018531) Product Usage: The Biomet Headless Compression Screws and Twist-Off…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 8, 2019
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), product code 35700BAX - Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
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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.