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 48,122 notices were distributed nationwide, so they reach Pennsylvania too — those are in the archive.
Reported Aug 31, 2016
CARESCAPE VC150 Vital Signs Monitor; Intended to monitor a single patient's vital signs at the site of care.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Innokas Medical Oy
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Large QWIX Compression screw, dia. 7.5 mm L 90 mm, Lot No. FH86, Rx only, Product Usage: The QWIX Positioning screw is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Medtronic, Viva Quadripolar Implantable Cardioverter Defibrillators: Product Model VIVAXTCRT-D DTBA1D1, DTBA1D4…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2016
RadSuite software. The firm name on the label is Merge Healthcare, Hartland, WI.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Radiesse (+) Lidocaine, Injectable Implant 1.5cc, Rx only, P/N: 8063M0K1, Merz Aesthetics. Product Usage: RADIESSE is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merz North America, Inc.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Brilliance 64 CT Model number 728231 Product Usage: Computed Tomography X-ray systems intended to produce…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Siemens RAPIDPoint¿ 500 v2.2.2A Software Upgrade Kit; SMN 11066719, Software Version 2.2A The RAPIDPoint 500 system is…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Siemens Healthcare Diagnostics Inc.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Infinite F50 instrument. The INFINITE F50 instrument is a 96-well absorbance reader for the measurement of light…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tecan US, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Ziehm Vision RFD 3D Mobile C-arm for Mobile Fluoroscopic Imaging
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ziehm Imaging Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 25, 2016
Sentry Foods Retira Productos De Pollo Congelados Por Posible Contaminacin Con Material Extrao
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Recalling firm not stated
USDA FSIS
Reported Aug 24, 2016
Bard TruGuide Disposable Coaxial Biopsy Needle Mixed Product Part Number C1816B The TruGuide Disposable Coaxial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Aug 24, 2016
Xpert MRSA Catalog GXMRSA-120, Rev. AJ Microbiology: The Cepheid Xpert MRSA assay performed in the GeneXpert Dx System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cepheid
FDA (openFDA device enforcement)
Reported Aug 24, 2016
Domino PURE CANE LARGE GRAIN GRANULATED SUGAR, NET WT 50 LB (22.67 kg), Distributed by Domino Foods, Inc., Yonkers, NY…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Domino Foods, Inc.
FDA (openFDA food enforcement)
Reported Aug 24, 2016
Al Rasheed Sardine Item #4017 Label not available - NYSDAM sampling.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Greenland Trading Corp.
FDA (openFDA food enforcement)
Reported Aug 24, 2016
Haitai Matdongsan Peanuts Crunch Snack, Net Wt. 11.49 oz. (325gr), Imported and Distributed by: Haitai, Inc, 7227…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.H & E Trading Inc.
FDA (openFDA food enforcement)
Reported Aug 24, 2016
Hospira RECEPTAL CANISTERS: 1L(1000mL), 1.5L(1500mL), 2L(2000mL) Canister, ATS, 2000, with Valve 1) List Numbers…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 24, 2016
OPTICAL BIOMETER AL-Scan: Software Version: 1.09 and earlier. Ophthalmic: The OPTICAL BIOMETER AL-Scan is a measuring…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nidek Inc.
FDA (openFDA device enforcement)
Reported Aug 24, 2016
TI Single Vector Distractor Body with Right Foot/20mm; Catalog ID 487.962 The Titanium Single Vector Distractor and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 24, 2016
Weck EFx Classic Fascial Closure System, Rx Only, Sterile, The product is intended to facilitate placement and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Aug 17, 2016
Snack Factory Original Pretzel Crisps, Thin, Crunchy Pretzel Crackers. Made in a facility that processes Milk and Soy.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baptista's Bakery, Inc.
FDA (openFDA food enforcement)
Reported Aug 17, 2016
BD Tritest CD3 FITC/CD4 PE/CD45 PerCP (IVD); Catalog number 340383. Label states: Contains CD3 FITC/CD4 PE/CD45 per CP…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
Reported Aug 17, 2016
NucliSENS easyMAG Magnetic Silica The NucliSENS easyMAG accessory products are reagents and disposable to be used with…
High riskUsing this product could cause serious injury, illness or death — stop using it now.BioMerieux SA
FDA (openFDA device enforcement)
Reported Aug 17, 2016
Medivance ArcticGel Neonatal Pad The pad is designed to fit into an incubator and provide whole body cooling for…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Aug 17, 2016
Hitachi Scenaria Computed Tomography System Hitachi Medical Systems America, Twinsburg, OH 44087
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.