All recall categories

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.

4,064 stored notices name Maryland, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,853 notices were distributed nationwide, so they reach Maryland too — those are in the archive.

Food

Reported Oct 2, 2013

JAMES FARM brand CUT GREEN BEANS (EJOTES CORTADOS), FRESH FROZEN, NET WT. 32 OZ. (2 LBS.) 907 g, UPC 7 60695 01004 2,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Restaurant Depot

FDA (openFDA food enforcement)

Food

Reported Oct 2, 2013

Fresh Herbs Everyday Basil, Shenandoah Growers brand, packaged in .75 oz; 2 oz.; and 2.5 oz. in 3 count and 6 count…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Shenandoah Growers, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 2, 2013

Smith Medical, Deltec, REF 21-2386-24, 11 Fr Introducer Set with Peel-Away Sheath, Sterile EO, Rx Only PORT-A-CATH¿ and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Smiths Medical ASD, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2013

Reliance Endoscope Processing System (REPS), STERIS Corporation, 5960 Heisley Road, Mentor, OH 44060-1834 USA…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Steris Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2013

Stryker Vision Mounting Arm, for use with other Stryker Endoscopy medical device products for human patients. Model…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2013

3M Scotchcast, Wet or Dry Cast Padding, Catalog Numbers WDP2, WDP3, WDP4, and WDP6. Intended for use in constructing…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

3M Company - Health Care Business

FDA (openFDA device enforcement)

Food

Reported Sep 25, 2013

Liquid Yeast Cream, Bulk, in tanker truck quantities, refrigerated 33F-45F

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

American Yeast Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Sep 25, 2013

Outlook ES pump is intended for use with B. Braun Medical Inc. Horizon Pump IV Sets. Used to regulate the flow of…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

B Braun Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2013

Osseotite 2 Certain Prevail 5mm(D)X 4.1mm (P) X X 11.5mm (L) Dental Implant Product Usage: Surgical placement in the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biomet 3i, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 25, 2013

Olde Cape Cod Chipotle Ranch dressing, 16 oz. Item Number: 90997-11630

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Cains Foods LP

FDA (openFDA food enforcement)

Medical devices

Reported Sep 25, 2013

C2244.3808, CONELOG Titanium Base CC ¿3.8GH0.8 inkl HS Product Usage: Endosseous dental implant abutment CONELOG…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Camlog USA

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2013

Vygon 14 Microbore Extension Set with Bionector, CMS-814-1. The CMS-814-1 is a 14 inch extension set used to administer…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Churchill Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2013

Blanketrol III, Model Number 233, Cincinnati Sub-Zero Products, Inc., 12011 Mosteller Road, Cincinnati, OH 45241…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cincinnati Sub-Zero Products Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2013

Cypher MIS Screw System, Biomet Spine Parsippany, NJ 07054. The Cypher MIS Screw System is a non-cervical spinal…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ebi, LLC

FDA (openFDA device enforcement)

Food

Reported Sep 25, 2013

Pills bury Cinnamon Rolls with Icing, CINNA BON, USPC 1800000501, 1800052230, 12.4 oz and 2-pack USPC 1800045675,2-…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

General Mills, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 25, 2013

ACL TOP (Base); PN 0000280000 Bench top, fully automated, random access analyzer designed specifically for in vitro…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Instrumentation Laboratory Co.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2013

Brilliance CT 6, M/N 728256; Brilliance CT 16 M/N 728246; Brilliance CT 40, M/N 728235 & Brilliance CT 64 M/N 728231,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2013

Sonogage EyeScan, A-Scan Biometer, Product Usage: A-Scan Biometer diagnostic device for measurement of axial eye length.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Sonogage Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2013

AEQUALIS Reversed II or AEQUALIS Reversed Fracture Impactor. These products are contained within the Aequalis reversed…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tornier, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2013

Juno DRF System. Mobile X-ray system These are general, multi-function x-ray systems capable of routine radiographs and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Villa Radiology Systems LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 18, 2013

OPERON D850 Surgical Table Product Usage: Surgical Table

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Berchtold Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 18, 2013

*** 1) Cat. 4341B; Qty. 10; Thoracentesis Tray; With Catheter; Sterile; CareFusion; 1500 Waukegan Road; McGaw Park, IL…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Carefusion 2200 Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 18, 2013

New Sun JLB Combination, Dietary Supplement, 100 capsule bottle, New Sun, Inc., Hendersonville, NC 1-800-544-0777…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

New Sun Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 18, 2013

Microscan Synergies Plus Negative Urine Combo 1 Product Usage: MicroScan¿ Synergies plus¿ Panels & MicroScan¿…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Siemens Healthcare Diagnostics, Inc.

10 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.