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.
Reported Sep 4, 2019
EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product Code:5905190, 14.5 Fr. Alphacurve Catheter with Standard Kit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
27 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 4, 2019
All colors and sizes of Confectionery Arts International, LLC brand Jewel Dust, a pearlescent pigment, manufactured and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Confectionery Arts International, LLC
FDA (openFDA food enforcement)
Reported Sep 4, 2019
EyeBOX Model OCL 02
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oculogica
FDA (openFDA device enforcement)
Reported Sep 4, 2019
Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is fully integrated and automated instrument including…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Phadia Ab
FDA (openFDA device enforcement)
Reported Aug 28, 2019
Brand Name Burn Navigator¿ Model Numbers: Catalog 1120, Burn Navigator¿ H2 Catalog 1125, Burn Navigator¿ H2 Transport…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arcos, Inc.
FDA (openFDA device enforcement)
Reported Aug 28, 2019
Kit BD Max Check-Points CPO IVD EU; Catalog # 278102
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
18 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 28, 2019
Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Ultra Delivery System) (20 mm) 9630TF20…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Edwards Lifesciences, LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 28, 2019
ABL90 FLEX Analyzer REF 393090 UDI:05700693930909
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Aug 28, 2019
ACUSON NX2 Diagnostic Ultrasound System, Model # 11284381, RX Only, Siemens Medical Solutions, containing software…
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 Aug 28, 2019
MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914
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 Aug 28, 2019
SIGA Fresh Basil, 1 lb bag, 10 plastic bags (1 lb bag) per carton
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siga Logistics S de Rl de Cv
FDA (openFDA food enforcement)
Reported Aug 21, 2019
Amy's Bowls - Broccoli & Cheddar Bake; Net Wt. 9.5 oz. (269g) Perishable - Keep Frozen. Microwave or regular oven. UPC:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amys Kitchen Inc.
FDA (openFDA food enforcement)
Reported Aug 21, 2019
Entenmann's Little Bites Soft Baked Cookies (5 pack Mini Chocolate Chip variety) Net Weight of 5ct box 6.88oz. 5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BIMBO Bakeries USA Inc.
FDA (openFDA food enforcement)
Reported Aug 21, 2019
K-Wire HBS Sterile, Item Number 19688 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioPro, Inc.
20 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 21, 2019
iGUIDE System with software build iGuide 2.2.0, 2.2.1, and 2.2.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Aug 21, 2019
Aries Bordetella Assay, REF 50-10037, UDI # 00840487101452
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 21, 2019
Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151810
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Alinity i Ferritin Reagent Kit, List Number 07P6530 The Alinity i Ferritin assay is a chemiluminescent microparticle…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Ireland Diagnostics Division
FDA (openFDA device enforcement)
Reported Aug 14, 2019
STERILE GRAVES VAGINAL SPECULUM MEDIUM Kit Code # GVS10MST - Product Usage:The speculum is used to spread the walls of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
12 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2019
IDEAL IMPLANT Structured Breast Implant, saline breast implant, in the following sizes: 210cc, 240cc, 270cc, 300cc,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ideal Implant Incorporated
FDA (openFDA device enforcement)
Reported Aug 14, 2019
SmartRelease Endoscopic Carpal Tunnel Release Handpiece (ECTR handpiece), part numbers 81014 and 83014
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MicroAire Surgical Instruments, LLC
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Human Assayed Multi-Sera Level 2, Model NO. HN1530 Product Usage: This product is intended for in vitro diagnostic use,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories, Limited
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Dimension¿ Ferritin (FERR) Flex¿ reagent cartridge DM FERR Product Usage: The FERR Flex reagent cartridge is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Shirakiku FISH CAKE IWASHI TEN SK F 20/150 g; Net WT. 5.29 oz. Keep frozen, 7 pcs. UPC 074410925246 Distributed by…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wismettac Asian Foods, Inc.
7 more products in this recall
FDA (openFDA food 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.