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 48,132 notices were distributed nationwide, so they reach Maryland too — those are in the archive.
Reported Jun 19, 2013
TX1 Tissue Removal System disposable handpieces. Product Usage: The TX1 Tissue Removal System is indicated for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Optisurgical Inc.
FDA (openFDA device enforcement)
Reported Jun 19, 2013
XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function, 90 and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Atlantic Pro Nutrients, Inc. dba XYMOGEN
FDA (openFDA food enforcement)
Reported Jun 19, 2013
embla Embletta Gold (It functions as a Polysomnography Recorder and Ventilator Effort Recorder). The Embletta Gold is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Embla System LLC
FDA (openFDA device enforcement)
Reported Jun 19, 2013
Chicken Noodle Soup Mix, "9 oz cello bag, Contents: All natural enriched semolina flour***PURELY AMERICAN 5991…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Purely American, Inc.
10 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 19, 2013
Trophy Nut Brand 1.5 oz. tube; Trophy Nut Brand 1.25 oz. tube; Nut Barrel Brand 5 oz. Fundraising bag; and Nut Barrel…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Trophy Nut Co. Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 12, 2013
FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS FLEXSTENT Biliary SES product is indicated for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2013
Cottage Cheese with Chive distributed under the following labels and sizes: (a) Hood brand Cottage Cheese with Chive,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HP Hood LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 12, 2013
Comfort brand Ear-Loop Face Mask, Item #: 3100, Model Numbers: # 3100B, # 3100P, # 3100G, # 3100Y, # 3100W; Product is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maytex Corp.
FDA (openFDA device enforcement)
Reported Jun 12, 2013
REF 8229705 x1 NIM TriVantage EMG Endotracheal Tube 5.0 mm I.D. x 6.5 mm O.D. Medtronic Xomed, Inc., 6743 Southpoint…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Xomed, Inc.
FDA (openFDA device enforcement)
Reported Jun 12, 2013
BrightView SPECT gamma camera for Emission Computed Tomography, Philips Medical Systems, Cleveland, OH 44143 BrightView…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jun 5, 2013
AngioDynamics Micro Introducer Kits under the following labeling: 1) AngioDynamics 4F Standard Micro-Introducer Kit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2013
Integrity 3.0 Product Usage: The Agility multileaf collimator is indicated for use when additional flexibility is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jun 5, 2013
EZ Breathe Atomizer Model # EZ-100. For the delivery of liquid medications for respiratory usage.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nephron Pharmaceuticals Corp.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2013
Femoral component, CR, cemented, #1, left 2103-1310 Femoral component, CR, cemented, #2, left 2103-1320 Femoral…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthopedic Alliance LLC
8 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2013
Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument - Aliquot Plunger Delivery System, 4", Part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthovita, Inc., dba Stryker Orthobiologics.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2013
45 mm Screw, Item #BG7045 Product Usage: Spinal Solutions distributes a variety of spinal fixation devices in loaner…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spinal Solutions, LLC
9 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2013
***REF S-3D*** 3mm Diamond Ball. Used for cutting and shaping bone.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
FDA (openFDA device enforcement)
Reported May 29, 2013
Rite Aid brand Maximum Strength Tussin Cough & Cold Mucus Relief CF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Aaron Industries Inc.
FDA (openFDA drug enforcement)
Reported May 29, 2013
Cardinal Health hCG Cassette Rapid Test, Part Number: B1077-22 (Mfg PN: 4582105026) The SP hCG Cassette Rapid Test is a…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Alere San Diego, Inc.
FDA (openFDA device enforcement)
Reported May 29, 2013
MyRay RXDC dental unit x-ray unit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cefla Dental Group
FDA (openFDA device enforcement)
Reported May 29, 2013
Rostorelle L, Polypropylene Mesh, Catalog number 501440, Manufacturer Coloplast A/S 3050 Denmark.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coloplast Manufacturing US, LLC
FDA (openFDA device enforcement)
Reported May 29, 2013
Krinos TAHINI ground sesame seeds, 1) Net. Wt. 1 lb (454g) in glass jars with gold lids packed 12 jars per case - UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Krinos Foods, Inc.
FDA (openFDA food enforcement)
Reported May 29, 2013
Ref: VP1600 HD Still Capture System ConMed Linvatec . Captures, stores and transfers images generated by a medical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Linvatec Corp. dba ConMed Linvatec
FDA (openFDA device enforcement)
Reported May 29, 2013
Brilliance CT 16-Slice Water, System Code: 728245; Brilliance CT 10-Slice Water, System Code: 728250; Brilliance CT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
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.