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 Apr 20, 2016
Blue Ridge Farms Vinegar & Oil Cole Slaw, 03010, Net Weight: 1 X 10 LB., Keep Refrigerated; Use by: 3/09/16, 3/20/16,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Winter Gardens Quality Foods, Inc.
9 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 20, 2016
X-Guide Surgical Navigation System, X-Clip Bulk Kit The X-Guide Surgical Navigation System is a computerized…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.X-NAV Technologies, LLC
FDA (openFDA device enforcement)
Reported Apr 13, 2016
Cittero Mortadella, packaged in deli bags. This is a deli service item.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bj Wholesale Club
70 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 13, 2016
GE Inspection Technologies, LP, Cabinet X-ray system used for industrial quality control.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Inspection Technologies, LP
FDA (openFDA device enforcement)
Reported Apr 13, 2016
Chef Hon brand STEAMED BUNS WITH SEAFOOD & VEGETABLE, Net Wt. 1 lb. 8 oz. (682g), UPC 7 47518 00156 2, Product Code #…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Peking Food LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 13, 2016
TeleSentry Battery, 3.7 Li-Ion Polymer Battery, CAUTION Do not expose to high temperature. Do not disassemble. Dispose…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Scottcare Corporation
FDA (openFDA device enforcement)
Reported Apr 13, 2016
A Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Apr 13, 2016
Guardian II Hemostasis Valve, models 8210 and 8211. The following models are only available Outside the US: FH101,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2016
The Spectra-System Dental Implant 2008 system is comprised of dental implant fixtures and prosthetic devices that…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Apr 6, 2016
MAGGI Chicken Flavor Bouillon 6Tab, 12Tab UPC Codes: 028000247959, 028000115678, 028000115678
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle USA
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 6, 2016
Knee Shield (Patella Cup) Product Usage: Knee Shield patella cup is an accessory used with the knee braces to provide…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur H / F
13 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2016
The E.CAM gamma camera system Product Usage: The E.CAM gamma camera system is a SPECT system and measures the…
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 6, 2016
Cios Alpha, mobile X-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
15 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Synthes Interlocking Bolt, 151 mm (General and Plastics Surgery Devices) Guide, Surgical Instrument
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Mar 30, 2016
Arthrex IBalance TKA Tibial Tray Size 2 - Catalog # AR-503-TTTC, Size 3 - Catalog # AR-503-TTTD, Size 4 -Catalog #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Mar 30, 2016
Alaris PC Unit, Infusion Pump Model 8000, Part No. TC10005092
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Mar 30, 2016
Universal Clamp¿ System (IFU reference: SNA027-N-90001). Provides the stability required for solid bone fusion and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Spine, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 23, 2016
CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM The product includes a Catheter Sheath Introducer (CSI) and a vessel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Mar 23, 2016
Intra operative MRI Systems: Neuro II-SE , Neuro III-SV, iMRI 1.5T A, and iMRI 3T S. Indicated for use as a magnetic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Deerfield Imaging
FDA (openFDA device enforcement)
Reported Mar 23, 2016
McKesson Horizon Medical Imaging (HMI) products versions 4.6.1 to including 11.9 and McKesson Radiology (MR) products…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Medical Immaging
FDA (openFDA device enforcement)
Reported Mar 23, 2016
Accu-Chek Inform II Base Unit as a part of the Accu-Chek Inform II Blood Glucose Monitoring System Accu-Chek inform II…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Mar 23, 2016
Siemens Syngo Dynamics-a Picture Archiving and Communication System (PACS) Model Numbers: 10091805, 10091807, 10091637,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Super Arrow-Flex Percutaneous Sheath Introducer Sets REF CL-07035 or CL-07635 or CL-07735 or CL-07835 Super Arrow-Flex…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J; Indicated for use in the prevention of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
1 more product 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.