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 8, 2019
FilmArray Gastrointestinal (GI) Panel, IVD, Rx Only, Biofire Diagnostics, LLC REF: RFIT-ASY-0104, and RFIT-ASY-0116),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported May 8, 2019
Lamb s Supreme Potato Tater Puffs, item # H30, packaged in 5-pound unprinted KRAFT paper bags, 6 bags to a case, sold…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lamb Weston BSW LLC
FDA (openFDA food enforcement)
Reported May 8, 2019
Ethyl Alcohol Enzymatic Assay, (a) REF 0220 (small test kit), (b) REF 0221 (large test kit) Product Usage: Detergent…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lin-Zhi International Inc.
FDA (openFDA device enforcement)
Reported May 8, 2019
EZ Derm Porcine Xenograft, labeled as the following: a. EZ Derm 3x4 (8x10 cm) Non-Perforated, Part Number: 131703-03;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Molnlycke Health Care, Inc.
FDA (openFDA device enforcement)
Reported May 8, 2019
cobas e 801 immunoassay analyzer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Corporation
FDA (openFDA device enforcement)
Reported May 1, 2019
Arthrex Burr, Oval, 12 Flute, 5.5 mm x 13 cm (AR-8550OBT) These devices are indicated for resection of soft and osseous…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported May 1, 2019
RT Elements Software revisions of the RT Elements applications have a specific software version number. Specifically…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported May 1, 2019
Edwards Lifesciences, Fogarty Dilation Atrioseptostomy Catheter, Sterile EO, Rx Only, REF: 830705F Product Usage: The…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Edwards Lifesciences, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 1, 2019
Performance Series Sagittal Blade, Catalog Number 6125-127-100 Product Usage: The Stryker Heavy Duty Sagittal Blades…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported May 1, 2019
Chips & Chocolate, A layered dessert with chocolate mousse layer on the bottom, with a white whipped topping layer on…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Winter Gardens Quality Foods, Inc.
FDA (openFDA food enforcement)
Reported Apr 24, 2019
FilmArray BCID Panel, IVD, Rx Only, BioFire Diagnostics, REF: RFIT-ASY-0126, and RFIT-ASY-0127, when used with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Apr 24, 2019
BIOVENTUS Bioactive Bone Graft Putty 15g Rx only/sterile. Filler device intended for use in bony voids or gaps that are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bioventus, LLC
FDA (openFDA device enforcement)
Reported Apr 24, 2019
Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding catheter is intended for use for…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cordis Corporation
FDA (openFDA device enforcement)
Reported Apr 24, 2019
Salto Talaris, Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 0, Right, Part No. LJU200T
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
25 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 24, 2019
NadaMoo! Strawberry Cheesecake Non-Dairy Frozen-Dessert 16 ounce/pint packaged in a carton
High riskUsing this product could cause serious injury, illness or death — stop using it now.Little Red Rooster Company
FDA (openFDA food enforcement)
Reported Apr 24, 2019
Obturator (long cone), Part number 25162 Product Usage: The obturator is a component of the Flex Rectoscope which is an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medrobotics Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 24, 2019
Acusnare Polypectomy (Duck Bill Shaped) Snare Used with an electrosurgical unit for endoscopic polypectomy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wilson-Cook Medical Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2019
Gravity IV Set with 3-port Closed Stopcock Manifold Model CS42522E-07
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 17, 2019
CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD), Pro. Code L20431 Product Usage: The affected CORAIL Neck Trials are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 17, 2019
Impossible Foods Bulk, 5 lb. vacuum sealed plastic-pack. Keep Frozen; This is a plant product that is looks like and is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Impossible Foods
FDA (openFDA food enforcement)
Reported Apr 17, 2019
syngo.via syngo.CT Cardiac Function, Model Number 10496180 Product Usage: Syngo.CT Cardiac Planning and syngo CT.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 3, 2019
Accelerate Pheno system, with Accelerate Pheno System Software 1.2.1 - 1.3.1, PSW000012B Product Usage: The Accelerate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accelerate Diagnostics Inc.
FDA (openFDA device enforcement)
Reported Apr 3, 2019
Avitus¿ Bone Harvester w/ Filter Insert - 8mm intended to harvest cancellous bone and bone marrow Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Avitus Orthopaedics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 3, 2019
BVI Visitec Soft Tip Cannula, 0.8MM .50 x 33mm (25G x 1.3 in). The BVI Soft Tip Cannula is intended to irrigate and/or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beaver Visitec
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.