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 48,100 notices were distributed nationwide, so they reach Maryland too — those are in the archive.
Reported Oct 16, 2019
20" 2-Needle 26-Gauge 6mm HlgH-Flo Subcutaneous Safety Needle Sets" Product # RMS22606 - Product Usage: RMS HlgH-Flo…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Repro-Med Systems, Inc.
FDA (openFDA device enforcement)
Reported Oct 16, 2019
Online TDM Vancomycin Gen.3 (100 tests) Catalog # 06779336190 Analyzer/Module: cobas c 311 and cobas c 501/502
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 16, 2019
TriMed Dorsal Wrist Hook Plate, Dorsal, 4-Hole, REF WHD-4, contained in a tray, insert, or poly package containing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TriMed Inc.
FDA (openFDA device enforcement)
Reported Oct 9, 2019
L5C4531 X1 Integrated APD Set with Cassette 3-Prong Sterile, nonpyrogenic fluid path. Sterilized by ethylene oxide.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Oct 9, 2019
Gold Medal Enriched, Presifted, Unbleached All Purpose Flour, Net Wt. 5 lb (2.26 kg), in paper bags. UPC 16000-19610
Moderate riskThis product could cause temporary or reversible health problems — stop using it.General Mills, Inc.
FDA (openFDA food enforcement)
Reported Oct 9, 2019
TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 LEFT Catalog # 5541-A-201 - Product Usage: Triathlon Femoral Distal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 9, 2019
ImplantDirect simply RePlant Implant, size 4.3mmD x 13mmL, 4.3mmD Platform, REF 604313U, Rx, Sterile. The firm name on…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 9, 2019
Paltop Advanced Plus Dental Implant Dia 6.0mm L10mm Catalog Number: 20-70024P
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Paltop Advanced Dental Solutions Ltd.
FDA (openFDA device enforcement)
Reported Oct 2, 2019
Gold Cup Leadwire and Snap Leadwire with the following component descriptions: 1. 24" Snap Leadwire, Blue; 2. 40" Snap…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GN Otometrics
FDA (openFDA device enforcement)
Reported Oct 2, 2019
Philips HeartStart Infant/Child SMART Pads Cartridge, Model # M5072A, UDI:00884838023758
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Oct 2, 2019
FuPaiYuan "***NOUGAT CANDIES***20190424***Candy***NET WT 450G (15.8oz)***INGREDIENTS Glucose syrup, sugar, peanut,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Rong Shing Trading NY Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 25, 2019
AD-TECH Drill Sleeve Guides, used with Ad-Tech Placement Kits: (a) REF DSG-90-2.3N (b) REF DSG-6.3-090-2.4N
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ad-Tech Medical Instrument Corporation
FDA (openFDA device enforcement)
Reported Sep 25, 2019
Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System, labeled as EMBLEMTM S-ICD Pulse Generator
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2019
LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Sep 25, 2019
MiCal brand YELLOWFIN TUNA POKE CUBE, Raw, Frozen, Product of Vietnam, Wild Caught. Cube size - 1 inch (2cm x 2cm) AAA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stavis Seafoods, Inc.
FDA (openFDA food enforcement)
Reported Sep 18, 2019
Natrelle, Saline-Filled Breast Implant Biocell Full Height with Fill Tube, Sterile, for the following style numbers:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Allergan PLC
14 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 18, 2019
Plastic Bottles labeled with: "Ancient Youth Secret - Since 500 B.C., DR. NARAM'S RASAYANA D TABLET, Calcium Supplement…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Jivan Shakti Inc.
FDA (openFDA food enforcement)
Reported Sep 18, 2019
PediaSmart Organic Soy Vanilla Beverage Mix, 12.7 oz. (360g) composite can
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natures One Inc.
FDA (openFDA food enforcement)
Reported Sep 18, 2019
Cracked Pepper Chicken of the Sea Wild-Caught Pink Salmon Skinless and Boneless, 2.5 oz (70 g) pouch: Shelf Stable UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tri-Union Frozen Products, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 18, 2019
XP- CR Tibial Tray- Interlok 59mm Item # 195268
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
34 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 11, 2019
Alere Cholestech LDX Analyzer, model # 14-874 containing power supplies with the identifying codes of 1837d and 1843d -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alere San Diego, Inc.
FDA (openFDA device enforcement)
Reported Sep 11, 2019
Norm-O-Temp model 111Z
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cincinnati Sub-Zero Products LLC, a Gentherm Company
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 11, 2019
OMNIlife science, Inc. ApeX acetabular liner hip prosthesis component Serf Dual Mobility Cup Liner 53-28; Product code:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OMNIlife science Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 11, 2019
Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel, a component of Berchtold Chromophare Ceiling Mounted…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Communications
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.