All recall categories

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.

Medical devices

Reported Jan 18, 2017

OPT Croutons is a synthetic bone substitute designed for the repair of bony defects and is made of pure beta-tricalcium…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Acumed LLC

FDA (openFDA device enforcement)

Food

Reported Jan 18, 2017

In The Mix¿ Monkey Bread Mix NET WT 16 oz (16 lb) 454 g box, INGREDIENTS: BREAD MIX: ***BUTTERMILK*** DISTRIBUTED BY…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Brand Castle LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jan 18, 2017

Oncentra External Beam Oncentra Brachy Product Usage: Oncentra is radiation therapy planning software designed to…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Elekta, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 18, 2017

Cardboard sleeve: Double Takes Macaroni & Cheese Dinner, Distributed By: Greenbrier International, Inc., 500 Volvo…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Fourth Street Barbeque, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 18, 2017

OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE OEC Medical Systems, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 18, 2017

House Autry, stone Ground Buttermilk Corn Bread Mix, Net wt. 8 oz. boxes, UPC Code 0 73484 15512 2,

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

House-Autry Mills, Inc.

6 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 18, 2017

Medline E-Z Lubricating Jelly; Bacteriostatic. Water Soluble. Sterile. 2 FL OZ (59 ml). Product Usage: For medical…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medline Ind

FDA (openFDA device enforcement)

Medical devices

Reported Jan 18, 2017

Merge Eye Station f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 18, 2017

NEW HOPE MILLS Crepe MIX, NET WT. 1 LB. 4 OZ, UPC 074703601529 --- 181 York Street, Auburn, New York 13021 ---Product…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

New Hope Mills Mfg., Inc.

FDA (openFDA food enforcement)

Food

Reported Jan 18, 2017

Starkey Spring Water, Item code STC.5, 16.9 FL oz. (500 mL) glass bottle. Product UPC 8 11904 02000 7. Case UPC 8 11904…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Starkey Water

FDA (openFDA food enforcement)

Medical devices

Reported Jan 18, 2017

Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT, CR3434CT Ablation catheter cables are designed as…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Sustainability Solutions

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 18, 2017

Non Fat Dry Milk, Grade A - High Heat in 50 # bags , manufactured by Valley Milk Products. Stasburg, Virginia 22657 ,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Valley Milk Products

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 18, 2017

VOCO Futurabond M+ adhesive, RF 1515, Manufactured by VOCO GmbH, Futurabond M+ is a dental adhesive for use with…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Voco GmbH

FDA (openFDA device enforcement)

Food

Reported Jan 11, 2017

Big Red Fresh Tomatoes, 5x6/6x6/6x7, 25 lb cardboard boxes. Distributed by Big Red Tomatoes. Kept refrigerated.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Big Red Tomato Packers, LLC

FDA (openFDA food enforcement)

Food

Reported Jan 11, 2017

AMERICAN CLASSIC SUB Net Wt 6.5 oz (184g) Smoked ham, deli style bologna, hard salami with American and Swiss cheese on…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Eby Brown Co.

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

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)

Medical devices

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)

Food

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

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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.