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 Jun 10, 2020
Pressure Monitoring Set, C-PMS, G02838
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2020
System, Tomography Computed Emmission
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2020
da Vinci SP surgical system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jun 10, 2020
OSTEOVATIONEX 2CC INJECT FORMULA. REF/UDI: 390-0002/00813845020009 - Product Usage: The product provides a bone void…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Osteomed, LLC
11 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2020
safeCLINITUBES Blood Sampler;REF 942-892;D957P-70-100x1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 3, 2020
Epix latis GRASPER, 5 mm x 35 cm, REF C4130, Qty: 10, Sterile R, CE, Rx ONLY, UDI: (01)00607915110147
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Applied Medical Resources Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 3, 2020
ISE Electrolyte Reference (2 X 2L) Reagent, REF A28937, UDI: 15099590202491 - Product Usage: are intended for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Jun 3, 2020
Giraffe Shuttle. Upgrade Kits with part number 2109672-001 and 2109673-001 GTIN: 00840682110808.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jun 3, 2020
GENTLEWAVE REF: FG-002-0001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sonendo Inc.
FDA (openFDA device enforcement)
Reported Jun 3, 2020
Optilite Optilite Rheumatoid Factor Kit, Ref: LK151.OPT.A, IVD, Rx Only, UDI: 05051700020015 (kit ea. containing four…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Binding Site Group, Ltd.
FDA (openFDA device enforcement)
Reported Jun 3, 2020
Wegmans Tuna Salad, 16 OZ (1 LB) 454 g; UPC: 77890-48147; SELL BY 5/21/20
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wegmans Food Markets, Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported May 27, 2020
AMS 700 100 mL, Spherical Reservoir with InhibiZone, Part No. 72404156 - Product Usage: intended for use in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported May 27, 2020
Frames Direct Prescription Spectacle Lenses included in the frame brands
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Frames Direct
FDA (openFDA device enforcement)
Reported May 27, 2020
Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 54 Left, Sterile, Catalog # 504-02-54C-L, UDI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
15 more products in this recall
FDA (openFDA device enforcement)
Reported May 27, 2020
K2M, ALEUTIAN Interbody Spacer Systems, EN AN Lordotic Spreader, Stainless Steel, Non-Sterile, Qty 1, Catalog #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.K2M, Inc.
23 more products in this recall
FDA (openFDA device enforcement)
Reported May 27, 2020
Wegmans brand Semi-Sweet Chocolate Nonpareils in an 18.5 oz. (524 g) plastic container, 12 plastic containers per case.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mellace Family Brands California Inc.
FDA (openFDA food enforcement)
Reported May 20, 2020
BARD Access Systems PowerPort ClearVUE Slim Implantable Port With Smooth Septum and Attachable 6 F Polyurethane…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported May 20, 2020
Analyte specific reagent. REF/UDI: 641408/641408-4012-1-1 (US); 641417/641417-1157-1-01 (OUS); 641399/641399-4012-1-01…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
Reported May 20, 2020
SureStep Foley Tray System - Product Usage: Intended for use in the drainage and/or collection and/or measurement of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard Inc.
FDA (openFDA device enforcement)
Reported May 20, 2020
DeRoyal Sterile Custom Kits packaged as a Piggy Back with the BD PosiFlush SF Saline Flush Syringe, labeled as follows:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
FDA (openFDA device enforcement)
Reported May 20, 2020
da Vinci Xi Surgical System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 20, 2020
Insufflation tubing to be used with varies insufflator units. REF 031200-10; REF 031322-10; REF 031532-10; REF 031622-10
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported May 20, 2020
Natural by Nature 1 % Milk (gallon, 1/2 gallon, and quart)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natural Dairy Products
2 more products in this recall
FDA (openFDA food enforcement)
Reported May 20, 2020
Philips Zenition 50, System code 718096 - Product Usage: The devices are used for radiological guidance and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Maryland recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
Other states
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.