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.
Reported Sep 2, 2015
Rato Bhale Nepali Finger Chips Product of Nepal Weight: 200g (7.05 OZ) Imported by: Balajee Trade Link, LLC, PA USA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Balajee Trade Link LLC
FDA (openFDA food enforcement)
Reported Sep 2, 2015
ExacTrac 6.0.x Patient Positioning System, Radiation therapy. Intended to be used to place patients at an accurately…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Sep 2, 2015
Wheel caster set screw for Ferno iNX Wheeled Stretcher. Ferno iNX Wheeled Stretcher for pre-hospital patient transport.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ferno-Washington Inc.
FDA (openFDA device enforcement)
Reported Sep 2, 2015
Caesar Salad, #5.56 (2,522g) "INGREDIENTS: Romaine Lettuce, Caesar Dressing (Soybean oil, water, distilled vinegar,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresh Unlimited Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 2, 2015
Centricity PACS-IW with Universal Viewer Product Usage: The Centricity PACS-IW with Universal Viewer is a picture…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 2, 2015
HardyCHROM MRSA Cat no: G307 Lot no: H15155 Expires: 2015-08-13 Container Type: 15x100mm monoplate Packaged: 10…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hardy Diagnostics
FDA (openFDA device enforcement)
Reported Sep 2, 2015
Kale Crisps Zen Nori product is seaweed flavored dehydrated kale chip, sold under brand Veggie Evolution, each poly…
High riskUsing this product could cause serious injury, illness or death — stop using it now.It Takes A Village Foods, LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 2, 2015
Central Line >34 Weeks Kit . Cardiology department. The Central Line >34 Weeks Kit (DYNDC1987A) is intended for use on…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Sep 2, 2015
0.9% Sodium Chloride Injection, USP, 10mL in 12mL., Single use, Rx only, Sterile Solution.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MRP, LLC dba AMUSA
FDA (openFDA device enforcement)
Reported Sep 2, 2015
PTW UNIDOS webline: 1) REF T10023, 2) REF T10022 and 3) REF T10023 Firmware version 2.05. Dosimeter for radiation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PTW-Freiburg
FDA (openFDA device enforcement)
Reported Sep 2, 2015
Salto Talaris Tibial Guide, Part # MJU333 ,Tray/Kit Code YKAL11, Non sterile. Orthopedic Manual Surgical Instrument
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tornier, Inc.
FDA (openFDA device enforcement)
Reported Aug 26, 2015
American Science & Engineering Inc,Gemini Cabinet X-ray system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Science & Engineering, Inc.
FDA (openFDA device enforcement)
Reported Aug 26, 2015
BD Vacutainer SST Plus Blood Collection Tubes, 5.0 mL, 13 x 100 mm, Sterile. Provides a means of collecting,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6"), 10 Fr, (30/box), Product Code 51610. Intermittent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Alaris Medley LVP Frame Membrane. Intended use to hold platen assembly and help protect the bezel assembly's internal…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Elite Biomedical Solutions LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Friendly's Vienna Mocha Chunk Ice Cream Tub, 48 U.S. FL. OZ. UPC: 0-29839 00557-4
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Friendly Ice Cream Corp.
FDA (openFDA food enforcement)
Reported Aug 26, 2015
Getinge 86 Series Washer/Disinfector with G1 control system software, Model 8666 and Model 8668. For use in healthcare…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Getinge Disinfection Ab
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Frozen Jamba, Fruit & Veggie Smoothies, Green Fusion, Green Apple, Mango, Pineapple, Kiwi, Banana, Broccoli and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Inventure Foods
64 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 26, 2015
Medtronic EOPA Arterial Cannula, Model # 77620. Lot: 2015060544 intended to deliver oxygenated blood to the heart…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Siemens Symbia S Series system, a diagnostic analog or digital detector based planar (2- dimensional) nuclear medicine…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Bronchial Double Lumen Tube Set (Left), Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
2.0/2.4 Cannulated Screw Countersink Part # 210-24-002 NON-STERILE and 3.0/4.0 Cannulated Screw Countersink Part #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical Ltd.
FDA (openFDA device enforcement)
Reported Aug 19, 2015
GE Optional Laser Centering Device X-ray generator.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Inspection Technologies, LP
FDA (openFDA device enforcement)
Reported Aug 19, 2015
Oasis Coil Extension Cable used with Hitachi Oasis MRI System Product Usage: The Oasis MR system is an imaging device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America 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.