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.
5,896 stored notices name Pennsylvania, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Pennsylvania too — those are in the archive.
Reported Jul 8, 2020
Control Panel REF - 60-02-50: LivaNova SCP Pump Control Panel S5/C5. REF 60-02-50, IPX2, RxOnly, UDI: 04033817900993
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova Deutschland GmbH
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2020
Sterile Disposable Connectors ASY CONN Y 1/2X1/2X3/8 STR 24. REF/ GTIN for Insert Label:029165000/ 00803622123153
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
21 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2020
ABL80-FLEX-393-839 Box Label, REF 393-839, IVD, CE, UDI: 05700693938394 - Product Usage: It is intended for use in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2020
Gordon Choice Imitation Crab Supreme Style, Net Wt 40 oz (2 lb 8 oz) Keep Frozen. UPC 93901-71212. For Distribution…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Trident Seafoods Corporation
FDA (openFDA food enforcement)
Reported Jul 1, 2020
BioPince Full Core Biopsy Instrument 16ga x 15cm.,Use with Optional CO-Axial Needle MCXS1615BP. QTY.: 5/CS - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Argon Medical Devices, Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2020
Xi Zhi Liang Fruit Jelly Cups; 21.1oz (600g); packaged in pink, yellow, and blue plastic backpacks with numerous…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Rong Shing Trading NY Inc.
FDA (openFDA food enforcement)
Reported Jul 1, 2020
Atellica Solution IM1300 Analyzer, Siemens Material Number 11066001, UDI # 00630414007960
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 1, 2020
Stumptown Cold Brew Coffee and Chocolate with Oatmilk. Product is TetraPak Prisma Pak aseptic packaging. Keep…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stumptown Coffee Corp.
FDA (openFDA food enforcement)
Reported Jul 1, 2020
Oscar 2, Model 250 System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Suntech Medical, Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2020
Piccolo Xpress chemistry analyzer, Model No. 1100-1001, Software version 2.1.55 (NGA)/3.1.35(Jen II)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abaxis Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2020
PENTARAY NAV HIGH-DENSITY MAPPING CATHETER ELECTRODE EA 22 Rx only STERILE EO - Product Usage: The Biosense Webster…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biosense Webster
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 24, 2020
Extremities, Large Kit Assy, US, 15/3 - Product Usage: is an injectable, moldable and biocompatible calcium phosphate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Sofamor Danek USA Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 24, 2020
VITROS Chemistry Product AMYL Slides Reagent, AMYLASE/5 PACK/300 SLDS, Product Code 1202670, UDI # 10758750008513 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 24, 2020
Heparin Sodium 5,000 units in 0.9% Sodium Chloride 1000 mL bag (5 units/mL), Rx Only, SCA Pharmaceuticals 755 Rainbow…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SCA Pharmaceuticals
FDA (openFDA drug enforcement)
Reported Jun 17, 2020
Acrysof, IQ IOL w/UltraSert System, AcrySof IQ ASPHERIC IOL, 20.5 D, SP ACRYLIC FOLDABLE LENS, w/UltraSert DELIVERY…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research LLC
FDA (openFDA device enforcement)
Reported Jun 17, 2020
BD FACS Sample Prep Assistant (SPA) II - Product Usage: K050191: The BD FACSCanto system with BD FACSCanto clinical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Biosciences
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2020
Infinix-8000V with Catheterization Table CAT-850B or CAT-860B - Product Usage: This device is a digital…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2020
Bin Butternut Squash, Bulk, Raw Product in Bins / 4, 5lb packages in each case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coastal Sunbelt Produce Co. Inc.
FDA (openFDA food enforcement)
Reported Jun 17, 2020
Healthy Choice Pesto and Egg bowls labeled in the following ways: 1) (for the US market) Healthy Choice Power Bowls…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConAgra Foods, Inc.
FDA (openFDA food enforcement)
Reported Jun 17, 2020
RadiForce GX560 monochrome LCD monitor, models 0FTD2347 and 0FTD2379 - Product Usage: is indicated for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eizo Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2020
Elekta Unity, Philips Marlin Software versions: R5.3.30, R5.3.31, R6.0.5331, R5.7.0, R5.7.1, R6.1.571
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta Limited
FDA (openFDA device enforcement)
Reported Jun 17, 2020
Elekta Unity, UDI 05060191071321, Image-guided radiation therapy system - Product Usage: is indicated for radiation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jun 17, 2020
Ovation iX Abdominal Stent Graft Systems, REF: TV-AB2080-I, TV-AB2080-J, TV-AB2380-I, TV-AB2380-J, TV-AB2680-I,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Endologix, Inc.
FDA (openFDA device enforcement)
Reported Jun 17, 2020
Triever20 Aspiration Guide Catheter a component of FlowTriever Retrieval/ Aspiration System, UDI: 00850291007079
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Inari Medical
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.