Recalls distributed in Pennsylvania
These notices name Pennsylvania 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.
5,899 stored notices name Pennsylvania, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,828 notices were distributed nationwide, so they reach Pennsylvania too — those are in the archive.
Reported Nov 28, 2018
Signature Select Mexican Style Roasted Corn; 12 oz.; 12/12oz. units per case; Keep Frozen Until Ready To Use; UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Harvest Food Group
2 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 28, 2018
Irrisept OR, Finished Bottle Assembly 450 ml STEP 1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company
FDA (openFDA device enforcement)
Reported Nov 28, 2018
Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031 (Model: Minicon B-15) & 9051 (Model: Minicon…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merck Millipore Ltd.
FDA (openFDA device enforcement)
Reported Nov 28, 2018
PremierPro Aluminum Adjustable Walker
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Svs LLC
FDA (openFDA device enforcement)
Reported Nov 28, 2018
Binding Site Human IgM Kit (for SPAPLUS), REF: NK012.S The device consists of reaction buffer, sheep anti-IgM…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Binding Site Group, Ltd.
FDA (openFDA device enforcement)
Reported Nov 28, 2018
Southwest Style Vegetable & Quinoa Protein Blend; Corn, Farro, Brown Rice, Red Bell Peppers, Black Beans, Poblano…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Perfect Bite Co.
FDA (openFDA food enforcement)
Reported Nov 28, 2018
AIA-2000 Analyzer, Model Nos. AIA-2000LA, AIA-2000ST - Product Usage: The AIA-2000 is capable of performing three…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Bioscience Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 21, 2018
Arrow AGB+ Multi-Lumen CVC Kit, 7 Fr., 3 Lumen, 20cm catheter length, .025 inch dia. spring-wire guide, Product Code…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Nov 21, 2018
3.2mm Proximal Reamer/Cannulated Drill provided as part of the Fibulock Fibular Nail System Pack. FibuLock Nail…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Nov 21, 2018
GE Healthcare Millennium MyoSIGHT Nuclear Cardiology Imaging System H3000ZH Acquisition System
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 21, 2018
VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as five-pack carriers) Product Usage: In vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
FDA (openFDA device enforcement)
Reported Nov 21, 2018
Rojo's Autentico Black Bean 5 Layer Dip; Layers of Black Beans, Guacamole, Salsa, sour Cream and Cheddar Cheese. NET…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Simply Fresh Foods, Inc.
FDA (openFDA food enforcement)
Reported Nov 21, 2018
Curry powder packaged under bulk, retail, and food service labels. Bulk: CURRY POWDER Net Weight 55 LBS, DISTRIBUTED BY…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sirob Imports, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 21, 2018
The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 21, 2018
Chef Sensations Fire Roasted 1/2" diced onion/pepper blend Net Wt 20 lbs
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Wornick Company
FDA (openFDA food enforcement)
Reported Nov 21, 2018
Wegmans Pumpkin Loaf, 19 oz., UPC 77890 27002
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wegmans Food Markets, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 21, 2018
Affixus Hip Fracture Nail Left Deg 9x300mm, Item Number 814609300 The Affixus Hip Fracture Nail System, comprised of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 14, 2018
Millville Maple & Brown Sugar Instant Oatmeal 15.1 oz. 10 individual serving size packets per 15.1oz retail unit. UPC:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aldi Inc.
FDA (openFDA food enforcement)
Reported Nov 14, 2018
BD NEXIVA Closed IV Catheter System Dual Port 18GA 1.25 IN (BD Nexiva Catheter), Catalog Number 383539 Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 14, 2018
ParaPost Plus 25 Titanium Alloy Spiral Vented and Serrated Posts Catalog Number: P2845B Dental Posts are implanted into…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coltene Whaledent Inc.
FDA (openFDA device enforcement)
Reported Nov 14, 2018
Cordis POWERFLEX PRO PTA Dilatation Catheter - Product Usage: Is intended to dilate stenoses in iliac, femoral,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Nov 14, 2018
Centricity PACS-IW with Universal Viewer version 5.0.x with PACS-IW foundation displays medical images (including…
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 Nov 14, 2018
FlareHawk Interbody Fusion System (previously XCage Interbody Fusion System) Instructions for Use (IFU's) only. Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integrity Implants Inc.
FDA (openFDA device enforcement)
Reported Nov 14, 2018
Fit & Active Southwest Veggie Stuffed Sandwiches NET WT 9 oz (255 g) KEEP FROZEN Distributed by ALDI Inc. Batavia, IL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.J&J Snack Foods Handheld Corp.
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.