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 48,828 notices were distributed nationwide, so they reach Maryland too — those are in the archive.
Reported Aug 3, 2016
Grossglockner Inc. Recalls Pork Products Due To Misbranding
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Grossglockner Inc.
USDA FSIS
Reported Aug 3, 2016
Harris Teeter Organics Mixed Vegetables, 16oz bags (product labeling not available).
High riskUsing this product could cause serious injury, illness or death — stop using it now.Harris Teeter Distribution Ctr
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 3, 2016
Syva¿ EMIT¿ 2000 Theophylline - Catalog # 4P019UL /SMN#10445324 is a homogeneous enzyme immunoassay intended for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 3, 2016
Stryker Orthopaedics Trident Constrained Liner Inserter/Impactor Tip, 22 mm, 28 mm, and 32 mm. Non Sterile Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported Aug 3, 2016
AUTOCOMP6 XPS High Speed Compounder REF 58810
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Metrix Company
7 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 27, 2016
Amerigel Hydrogel Wound Dressing Advanced Formula for wound management 1 oz.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amerx Health Care Corp.
FDA (openFDA device enforcement)
Reported Jul 27, 2016
BD Trucount Tubes: Catalog number: 340334 Hematology: BD Trucount tubes are used for determining absolute counts of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
Reported Jul 27, 2016
Frozen Organic Premium Sweet Baby Peas, Organic by Nature brand, net wt. 5 lb. The UPC is 8 46358 00063 3. Frozen IQF…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CRF Frozen Foods, LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 27, 2016
Dimension Vista¿ Homocysteine Flex Reagent Cartridge (HCYS), Device Listing No.: D017878 is an in vitro diagnostic test…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CSL Behring GmbH
FDA (openFDA device enforcement)
Reported Jul 27, 2016
ATEC CANISTER. Suction Canister with Lid 490 cc., RX Only; Suction canister used to collect fluid during a breast…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Jul 27, 2016
Kellogg's Special K Mini Brownies Blondie, 6 ct, 4.44 oz.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kellogg Company
24 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 27, 2016
Navitas Naturals Superfood Hemp bar: Creamy Peanut, Hemp, Nut Bar. Net Wt. 1.4 oz/40 G. Gluten free. Ingredients:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Navitas, LLC.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 27, 2016
ADVIA¿ Centaur XPT system software versions V1.0.1 (Bundle 1.0.912 SMN 10819704), V1.0.2 (Bundle 1.0.1086 SMN…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jul 27, 2016
Syngo.via, picture archiving and communications system software controlled. Intended to be used for viewing,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jul 27, 2016
AngioDynamics Soft Vu Omni Flush Angiographic Catheter Model Number: 10732203
High riskUsing this product could cause serious injury, illness or death — stop using it now.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Jul 27, 2016
Depuy Synthes Trauma- Trochanteric Fixation Nail Advanced (TFNA) Blade/Screw Guide Sleeve, Surgical Instrument Part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Jul 27, 2016
HX2" Temperature Management Systems; The Terumo¿ HX2" Temperature Management System provides temperature control of two…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 27, 2016
The pump (with cushioning foam inserts) is packaged in a single pump box. Four pump boxes are placed in an over-shipper…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.WalkMed Infusion, LLC
16 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2016
Mammotome Revolve Dual Vacuum Assist Biopsy System Model number: MST1009 & MST0815. Each disposable probe is packaged…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Devicor Medical Products Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2016
HeartWare Ventricular Assist System: HeartWare Battery, Lithium Ion, 14.8 V, Rx only. Catalog 1650 (US) and 1650,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heartware, Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2016
The LifeCare PCA Plus II infusion pump system is designed for safe, effective, analgesic delivery to patients through…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2016
Phenylephrine 40 mcg/mL injection in 0.9% Sodium Chloride 10 mL syringe, Rx Only, Compounded by PHARMAKON…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pharmakon Pharmaceuticals, Inc.
87 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 20, 2016
cobas¿ Liat Influenza A/B Quality Control Kit; For use with cobas¿ Liat Influenza A/B Assay.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Roche Molecular Systems, Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2016
6.5 mm Cannulated Screw, Product code HWC, Device Listing Number D028949, Screw, Fixation Bone Product Usage: Intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
17 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.