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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.

5,819 stored notices name Pennsylvania, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,123 notices were distributed nationwide, so they reach Pennsylvania too — those are in the archive.

Medical devices

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)

Medical devices

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)

Medical devices

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)

Food

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)

Food

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)

Medical devices

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)

Food

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)

Food

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)

Medical devices

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)

Food

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Food

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)

Medical devices

Reported Nov 14, 2018

REF VV19F Reinforced Dual Lumen Cannula, 19Fr., Sterile EO, DISPOSABLE: DO NOT RE-USE CE 0473 Product Usage: The OriGen…

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

OriGen Biomedical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 14, 2018

VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/2, Catalog Number 1453489 For in vitro diagnostic use only…

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

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Nov 14, 2018

EZ1 Advanced XL, Model Number: 9001492, GTIN: 04053228010760 Product Usage: The EZ1 Advanced XL is designed to perform…

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

Qiagen Sciences LLC

FDA (openFDA device enforcement)

Food

Reported Nov 14, 2018

Inshell R/S 21/25 US- Select Pistachios; NET WT. 25 lb. (11.34kg) Product of the USA Production Date: 8/2018 ARO…

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

Sam Dry Fruits and Enterprises Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 7, 2018

3M Fast Release Varnish, 5% Sodium Fluoride, Mint Flavor, Rx Only, single use. 200 pack, with each package containing 1…

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

3M Company - Health Care Business

FDA (openFDA device enforcement)

Medical devices

Reported Nov 7, 2018

Li-ion Battery Housing for AR-400 DrillSaw Sports 400 System Product Usage: The battery housing is used to house the…

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

Arthrex, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 7, 2018

EXACTAMIX Empty EVA Bags - 250 mL Product Usage: A plastic container used to hold large-volume sterile solutions to be…

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

Baxter Healthcare Corporation

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 7, 2018

BD Max Instrument Reader Spare Part, Catalog Number 8090369/443364, 44336409 (Repaired Reader spare part) - Product…

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

Becton Dickinson & Co.

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.