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.
4,062 stored notices name Maryland, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,842 notices were distributed nationwide, so they reach Maryland too — those are in the archive.
Reported Feb 19, 2014
The UF-1000i is a fully automated urine particle analyzer intended for vitro diagnostic use in urinalysis. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sysmex America, Inc.
FDA (openFDA device enforcement)
Reported Feb 12, 2014
XiO RTP System. Used to create treatment plans for any cancer patient for whom external beam radiation therapy or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Feb 12, 2014
Diagnostic imaging systems (GEMINI LXL Model #882412, TruFlight Select Model #882438, GEMINI TF PET/CT16 Model #882470,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2014
KODAK DirectView DR 7500 Dual Detector System, MODEL DR 7500, Manufactured by Carestream Health, Inc. Made in U.S.A.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carestream Health, Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2014
Kimberly-Clark RadiOpaque Radiofrequency Cannula, Gauge 22, Length 100 mm, Active Tip 10 mm, Distributed in the US by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kimberly-Clark Corporation
FDA (openFDA device enforcement)
Reported Feb 5, 2014
Port Kit with Access Infusion Set under the following labels: 1) 8F/SL/Plastic Port/F, Product Number H965450140,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Navilyst Medical, Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2014
Monarch Breakfast Syrup, in 1.5 oz. portion control cups, Distributed by US Foods, Inc., Rosemont, IL 60018.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sauer Company The C F
FDA (openFDA food enforcement)
Reported Feb 5, 2014
AnspacSingle use Sterile bone cutting burs.h REF: S-1504TD Twist Drill for 1.5mm x 4mm screw. Rx only Single use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 29, 2014
DRX-Evolution with FF WS These products are permanently installed diagnostic x-ray systems composed of 4 main…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carestream Health, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 29, 2014
Civco Belly Board, Reusable non-sterile carbon fiber belly board with cushion, REF 125012, packaged 1 per box. Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Civco Medical Instruments Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 29, 2014
Candy Place Chocolate Santas, in 11 oz clear plastic bags, individually wrapped assortment of double chocolate,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Giant Eagle
FDA (openFDA food enforcement)
Reported Jan 29, 2014
VITROS Chemistry Products COCM Reagent
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Jan 29, 2014
ADAC ARGUS Gamma Camera Systems & ADAC CIRRUS Gamma Camera Systems. Distributed by Philips Medical Systems, Cleveland,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 29, 2014
ABL90 FLEX Analyzer Radiometer Medical ApS, ¿kandevej 21 Br¿nsh¿j, Denmark A portable, automated analyzer that measures…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Jan 22, 2014
Shredded Swiss Cheese, INGREDIENTS: Milk, Cheese Culture, Enzymes......Aged 60 days. CONTAINS: MILK NET WT. 80 OZ. (5…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Biery Cheese Co.
FDA (openFDA food enforcement)
Reported Jan 22, 2014
Centricity PACS System versions 3.X and higher and 4.X and higher Product Usage: The Centricity PACS Workstation is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ge Healthcare It
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2014
Hot Smoked Wine Maple Salmon, Item HS-B, vacuum packaged and either frozen or refrigerated, ranging in size between…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Josephson's Smokehouse
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 22, 2014
Leica BIOSYSTEMS; BOND Polymer Refine Red Detection; Catalog No: DS9390; Leica Biosystems Newcastle Ltd; Balliol…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Biosystems Newcastle Ltd.
FDA (openFDA device enforcement)
Reported Jan 22, 2014
Oxoid Antimicrobial Susceptibility Testing Disc, MEM10, REF: CT0774B, 10 mcg meropenem, Packed in packs containing 5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
FDA (openFDA device enforcement)
Reported Jan 15, 2014
Sandel Healthcare Safety Devices Weighted Safety Scalpel #3 Disposable Safety Handle with #10 Blade Manufactured for:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ansell Sandel Medical Industries LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 15, 2014
SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed As GE Healthcare CARESCAPE Patient Data Module)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jan 15, 2014
Anspach BLACKMAX-N (Pneumatic motor) and Autolube III (Foot Control). Cutting and shaping bone.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 8, 2014
IntelliFill i.v. Pharmacy Compounding Device (PCD). Intended to fill syringes from 0.5mL up to 11.5mL using mixing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
FDA (openFDA device enforcement)
Reported Jan 8, 2014
Wegman's Brand New England Clam Chowder (refrigerated at 38F or below) in a 16 oz plastic cup.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Blount Fine Foods Corporation
FDA (openFDA food 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.