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.
5,900 stored notices name Pennsylvania, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,842 notices were distributed nationwide, so they reach Pennsylvania too — those are in the archive.
Reported Jan 11, 2017
G3 Opticage Expandable Interbody Fusion Device, Model No. 9180-00, 9180-01, 9180-06, 9180-07, 9180-17, 9101-00, 9101-06…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Interventional Spine Inc.
FDA (openFDA device enforcement)
Reported Jan 11, 2017
DR Systems Unity PACS software, now known as Merge Unity PACS software.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Jan 11, 2017
Refrigerated, Ready to Eat Herring in Brine with no brand name, packaged in bulk 25 lb. white plastic bucket and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Royal Seafood Baza, Inc.
16 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 4, 2017
Innova 2000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 4, 2017
Shimadzu X-ray TV System, Catalog No. SONIALVISION G4
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
CyberKnife Robotic Radiosurgery Systems, models: G3, G4, VSI. Radiology: The CyberKnife Robotic Radiosurgery System is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accuray Incorporated
FDA (openFDA device enforcement)
Reported Dec 28, 2016
ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Stiffened Micro-Introducer Kit, 45CM SS/SS…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Angiodynamics, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Gammex Non-Latex Sensitive Neoprene Surgical Gloves Ansell Lanka (pvt) Ltd. Biyagama Export Processing Zone, Biyagama,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ansell Healthcare Products LLC
FDA (openFDA device enforcement)
Reported Dec 28, 2016
BD SurePathTM Preservative Collection Vials, catalog numbers 490505, 490527, 491095, 491096, and 491097. SurePath¿…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Fresh Express Kit Caesar salad, Net Wt. 7.6 oz. (215g), Fresh Express Incorporated, 550 S. Caldwell St. Charlotte, NC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresh Express Incorpated
FDA (openFDA food enforcement)
Reported Dec 28, 2016
Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACAL CO., INC. Amityville, NY…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hi-Tech Pharmacal Co., Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 28, 2016
Girl Scout Peanut Butter Sandwich, NET WT 8 0Z (227 g). UPC 0 20200 07007 8, ABC Bakers/Interbake Foods LLC, Richmond,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Interbake Foods
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 28, 2016
Merge OrthoCase 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 Dec 28, 2016
Algovita Spinal Cord Stimulation System, Percutaneous Leads, 8-Electrode Percutaneous Lead Kit; Algovita Spinal Cord…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nuvectra
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Phil-Am Smoked Mackerel (Hasa Hasa) Net. Wt. 200g (7.05 oz.) packaged: Clear flexible plastic pouch and is topped by a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Phil-Am Trading, Inc.
FDA (openFDA food enforcement)
Reported Dec 28, 2016
CARPAL TUNNEL PACK, Surgical Instrument Tray, REF/Catalog No. 3366, STERILE, Rx Only -- busse Hospital Disposables…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Tibial Component Fixed Hinge Small Long; Tibial Component Fixed Hinge Small Short The product is a component is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stanmore Implants Worldwide Ltd.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
8450-107-530 3.0MM Precision Match Head, 13CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit including the Ultroid Disposable Sterile Probes
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ultroid Technologies, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
12 Gourmet Variety Pack Cookies - Net Wt. 15 oz UPC 289786003997 Gourmet Variety Pack Cookies Net Wt. 30 oz UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wakefern Food Corp.
18 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 28, 2016
CROISSANT 6 PK
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Whole Foods Market Brand 365, LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 28, 2016
Product is packaged into a plastic bag and placed into cardboard box. Product is labeled as "D'ALLESANDRO SALT-FREE…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Woodland Foods
5 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 21, 2016
CyberKnife Robotic Radiosurgery System using software version 10.6; Catalog/Part Number: 54000 UDI: M658053301 0…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accuray Incorporated
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.