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 May 16, 2018
MicroVue BAP EIA, Model 8012, provides a quantitative measure of bone-specific alkaline phosphatase (BAP) activity in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diagnostic Hybrids, Inc.
FDA (openFDA device enforcement)
Reported May 16, 2018
ZYMUTEST HIA MonoStrip IgG; REF Number: RK041A; UDI: 03663537046803 a qualitative assay intended for the detection of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hyphen BioMed
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 16, 2018
RESTORIS MCK TIBIAL BASEPLATE-RM/LL used in unicompartmental knee arthroplasty and knee replacements.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported May 16, 2018
Munk Pack PROTEIN COOKIE DOUBLE DARK CHOCOLATE NET WT 2.96oz (84g); UPC: 853787005368
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Munk Pack Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 16, 2018
Sugarfina Platinum Bling Ring; Product SKU No. R-1790 UPC: 840278116139 Net W. 21g ().7 oz.) Sculpted from dark…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Sugarfina, LLC
FDA (openFDA food enforcement)
Reported May 16, 2018
Raw Form Organics Maeng Da Kratom Emerald Green; 150 capsule and 300 capsule plastic bottles; Manufactured for Raw Form…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Triangle Pharmanaturals LLC
25 more products in this recall
FDA (openFDA food enforcement)
Reported May 9, 2018
Miriam Capsule Endoscope System. Model MR1100 Product Usage: MiroCam Capsule Endoscope System is intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.IntroMedic Co., Ltd.
FDA (openFDA device enforcement)
Reported May 9, 2018
Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision large screen monitor), Interventional fluoroscopic x-ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
FDA (openFDA device enforcement)
Reported May 2, 2018
Formagere de la Brie brand, l 'Explorateur, soft ripened cheese made from pasteurized milk, product comes in a 250g…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cheezwhse/Com
FDA (openFDA food enforcement)
Reported May 2, 2018
clariti 1 day/Fresh Day 90 pack (-1.00), UV Blocking, 90 silicon hydrogel, daily disposable contact lenses The Clariti…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.CooperVision Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 2, 2018
EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM, Product Number HEM3335, GTIN Number 1 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 2, 2018
Evicel Accessory Device - 45 cm Flexible Tip (SET OF 3), Product Code EVT45. Accessory Tips for use only with EVICEL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, Inc.
FDA (openFDA device enforcement)
Reported May 2, 2018
Triathlon Revision Knee Catalog #5545-A-301 and Catalog #5546-A-601 The knee system devices are sterile, single-use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 2, 2018
Shell Eggs packaged in quantities and styles of pack (plastic and pulp cartons, flats, and boxes)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Rose Acre Farm
FDA (openFDA food enforcement)
Reported May 2, 2018
Versatex Monofilament Mesh 50 x 50cm, Product No. VTX5050M The device is made out of a macroporous three-dimensional…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sofradim Production
FDA (openFDA device enforcement)
Reported Apr 25, 2018
Kratom capsules labeled in the following ways: 1) Divinity Kratom 10 Capsule Dietary Supplement, Divinity Product LLC,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Divinity Product Distribution LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 25, 2018
HUNGRY JACK Original PANCAKE & WAFFLE MIX NET WT 32 OZ (2 LB) 907 g
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The J.M. Smucker Company, Inc.
FDA (openFDA food enforcement)
Reported Apr 25, 2018
Zimmer Segmental System Proximal Femoral Component 38mm Offset, Model Number 00-5850-030-38 The Segmental System is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported Apr 18, 2018
AUTO REF/KERATOMETER ARK-1s
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nidek Inc.
FDA (openFDA device enforcement)
Reported Apr 18, 2018
Diet Pepsi; NOW ASPARTAME FREE; 6 PACK; 16 OZ BOTTLES; 6-16 FLOZ BOTTLES (96 FL OZ)
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Pepsi Cola Bottling Company
FDA (openFDA food enforcement)
Reported Apr 18, 2018
Magstim Rapid Therapy System consisting of: Rapid Mainframe, Rapid Single Power Supply Unit , Rapid User Interface, Air…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Magstim Company Limited
FDA (openFDA device enforcement)
Reported Apr 11, 2018
HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box, each catheter is packaged in an individual…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 11, 2018
Wegmans Yogurt Raisins, 9 OZ (255g), in a plastic tub, UPC: 0 77890 31832 4,
High riskUsing this product could cause serious injury, illness or death — stop using it now.First Source, LLC
FDA (openFDA food enforcement)
Reported Apr 11, 2018
2008 K2 Hemodialysis Machine with software version 5.40, Models: (1) Hemodialysis SYS OLC/Diasafe PLS 190610, UDI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Renal Therapies Group, LLC
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.