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.
5,903 stored notices name Pennsylvania, reported between Jun 20, 2012 and Nov 25, 2026. A further 48,868 notices were distributed nationwide, so they reach Pennsylvania too — those are in the archive.
Reported Feb 4, 2015
Thera Tablets with Beta Carotene Dietary Supplement
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.The Harvard Drug Group, LLC
FDA (openFDA food enforcement)
Reported Feb 4, 2015
Market Pantry Brand Dark Chocolate Covered Almonds 9 oz., UPC 085239555644
High riskUsing this product could cause serious injury, illness or death — stop using it now.Zachary Confections, Inc.
FDA (openFDA food enforcement)
Reported Jan 30, 2015
Pennsylvania Firm Recalls Pork Rib Products Due to Misbranding and Undeclared Allergen
High riskUsing this product could cause serious injury, illness or death — stop using it now.Clemens Food Group, LLC
USDA FSIS
Reported Jan 30, 2015
Ohio Firm Recalls Salami Products Due To Possible Temperature Abuse
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ohio Firm
USDA FSIS
Reported Jan 28, 2015
Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Jan 28, 2015
PF4 Concentrated Wash (10x), REF 403624, packaged in the following assay kits: 1. ImmucorGamma LIFECODES PF4 IgG…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Genetic Testing Institute,Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2015
Jumbo Lump Crab Cakes packed from bulk into clam shell containers with Giant Eagle scale label 100% Jumbo Lump Crab…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Giant Eagle, Inc.
FDA (openFDA food enforcement)
Reported Jan 28, 2015
TEGRIS System manufactured by MAQUET GMBH in Germany The Maquet Tegris OR Integration System is designed to be used as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Medical Systems USA
FDA (openFDA device enforcement)
Reported Jan 28, 2015
VITROS Software Version 3.1 utilized on the following systems: 1) 4600 Chemistry Systems (VITROS 5,1 FS System family…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Jan 28, 2015
Philips IntelliVue TcG10; Monitor, carbon-dioxide, cutaneous. The IntelliVue TcG10 is a device for the measurement of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2015
QuestBar Protein Bar Double Chocolate Chunk Flavor NET Wt. 2.12 OZ (60g) Lot #: 1BA4DCC14289 Exp Date: October 17, 2015…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quest Nutrition, LLC.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 28, 2015
Ysio Max, Luminos dRF Max and Agile Max systems with software version VE10 and SmartOrtho license. The Ysio Max is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
iPlan RT Dose is a stereotactic radiation treatment planning system that is intended for use in stereotactic,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Harvest Blend, Net Wt. 4 oz. (113g) Best If Enjoyed By: 12/05/2014, DISTRIBUTED BY 7-ELEVEN, INC., DALLAS, TX 75201 UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Del Monte Fresh Produce NA, Inc.
12 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 21, 2015
Civco, MTSR02 Shoulder Retractor with Sherpa Wrist Loops Kit with Base, Non-sterile re-usable wool wrist strap, REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Med Tec Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2015
POWEREASE Instruments Set Screw Breakoff Instrument, REF 2346010, Medtronic Sofamor Danek, USA, Inc. Spinal surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Sofamor Danek USA Inc.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
MENTOR MemoryGel Resterilizable Gel Sizer Moderate Plus Profile STERILE. Breast prosthesis sizer.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mentor Texas, LP.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Phadia 1000 Instrument (introduced as UniCAP 1000), Article number: 12-3800-01 (All instrument software versions since…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Phadia US Inc.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Various Brilliance and Ingenuity Computed Tomography X-ray systems; one unit per package Product Usage: Intended to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Artis zee/ zeego systems, model numbers: 10094135, 10094137, 10094139, 10094141, 10280959: dedicated angiography…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2015
EXp Tibial Insert ; Intended Use of Device(s): The Proven Gen-Flex Total Knee System is intended for: a. Total knee…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stelkast Co.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Drill set long, drill stop compatible for 4.8mm diameter implant, Article Number 040.447S Endosseous dental implant…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Straumann USA, LLC
FDA (openFDA device enforcement)
Reported Jan 21, 2015
The SurgiCounter Charging Cradle Product Usage: SurgiCounter Charging Cradles are designed to be used with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Femto LDV Z-Generation Femtosecond Surgical Lasers are used to perform ophthalmic surgeries.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ziemer USA Inc.
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.