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 Nov 14, 2018
Inshell R/S 21/25 US- Select Pistachios; NET WT. 25 lb. (11.34kg) Product of the USA Production Date: 8/2018 ARO…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sam Dry Fruits and Enterprises Inc.
FDA (openFDA food enforcement)
Reported Nov 7, 2018
Li-ion Battery Housing for AR-400 DrillSaw Sports 400 System Product Usage: The battery housing is used to house the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Nov 7, 2018
EXACTAMIX Empty EVA Bags - 250 mL Product Usage: A plastic container used to hold large-volume sterile solutions to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 7, 2018
BD Max Instrument Reader Spare Part, Catalog Number 8090369/443364, 44336409 (Repaired Reader spare part) - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 7, 2018
Houlihan's Creamy Garlic Ranch Dressing potentially labeled as Horseradish Sauce, 1 gal containers Mfg. exclusively…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CFS West Holdings Inc.
FDA (openFDA food enforcement)
Reported Nov 7, 2018
Zilver 518 Biliary Stent 4mm x 20mm, Catalog Number: ZIB5-125-4.0-20 Product Usage: The Zilver 518 and 635 Biliary…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Medical Incorporated
38 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 7, 2018
Spinach and Mushroom Pie, Net Wt. 6 OZ, packaged in a paper carton, Keep Frozen
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lone Star Bakery, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 7, 2018
SUGAR MELON CANDY / WAX GOURD The product comes in a 7.04oz plastics package marked with barcode 6912567116718.
High riskUsing this product could cause serious injury, illness or death — stop using it now.SLR FOOD Distribution, Inc.
FDA (openFDA food enforcement)
Reported Nov 7, 2018
Hoffman LRF Hexapod Strut, Extra Short 89mm-109mm, Model Number 4935-0-010. Product Usage - The Hoffmann LRF System is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker GmbH
3 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 7, 2018
Wegmans Hummus, NET WT 32 OZ (2 LB) 908g, UPC: 77890-26221 and NET WT 8 OZ (227g), UPC: 77890-26213
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wegmans Food Markets, Inc.
FDA (openFDA food enforcement)
Reported Nov 7, 2018
EBI Osteogen Implantable Bone Growth Stimulator The OsteoGen Implantable Bone Growth Stimulator is indicated in the…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2018
NucliSENS¿ Magnetic Extraction Reagents
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported Oct 31, 2018
Boston Scientific Maestro 4000 Cardiac Ablation System, Firmware Version 5.14, Model Numbers: M00440000, M0044000D0,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Oct 31, 2018
J-Plasma Precise 360, single use, disposable. The Bovie J-Plasma Precise 360 Handpiece is used for the delivery of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bovie Medical Corporation
FDA (openFDA device enforcement)
Reported Oct 31, 2018
Callie's Charleston Biscuits COCKTAIL HAM BISCUITS; 24 NET WT. 35 OZ (980 g) Callie's Charleston Biscuits; 1895 Avenue…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Callie's Charleston Biscuits
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 31, 2018
Nuclear Magnetic Resonance Imaging Systems that are indicated for use as a diagnostic imaging modality that produces…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
FDA (openFDA device enforcement)
Reported Oct 31, 2018
Cedar's Chickpea Salad, packaged in an 8oz plastic container, UPC: 044115337767. Product is refrigerated.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cedar's Mediterranean Foods, Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 31, 2018
CHS Custom Convenience Kit-DR. NANDA CLOSING TRAY(CONMED HYFRECATOR SHARP) Product Number: B9-15934B
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Custom Healthcare Systems, Inc.
28 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2018
Instrument Arm Drape (Box of 20) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively on the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ecolab Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2018
GE Healthcare, Discovery 3.0T MR750, 5148810-2, 5373011-2, 5499460-2.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2018Updated Oct 23, 2026
Les Aliments O Sole Mio, Inc., Recalls Poultry Products Produced without Benefit of Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Les Aliments O Sole Mio, Inc.,
USDA FSIS
Reported Oct 31, 2018
O-arm 1000 2nd Edition Imaging System, OARM ASSY Bl70000027 SYSTEM PRODUCT, Model Number Bl70000027 Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.-Littleton
9 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2018
APTIO INPUT/OUTPUT MODULE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 24, 2018
GE Healthcare MRI Systems, Software Version 11.x, sold under the following product names: 1.5T CXK4 LCC MAGNET,1.5T…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
2 more products in this recall
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.