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.

5,899 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.

Food

Reported Aug 15, 2018

Ocean Delight Individually Vacuum Packed AHI TUNA SAKU, 8-12 oz. NET WT. 10 LB (4.54 kg) and 12-16 oz. NET WT. 22LB…

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

Stavis Seafoods, Inc.

FDA (openFDA food enforcement)

Food

Reported Aug 15, 2018

utz Carolina Style Barbeque Potato Chips, Net Wt 2.875 OZ, UTZ Quality Foods, LLV, Hanover, PA 17301, UPC:…

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

Utz Quality Food Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 15, 2018

Waterpik Sonic-Fusion Professional, Model: SF-02 Product Usage: The device is composed of a unit base and an oral…

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

Water Pik, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

MicroScan Pos Combo Panel Type 43, Catalog number B1017-217for use in determining antimicrobial agent susceptibility…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 8, 2018

PINK LEMONADE COOKIES Byrd's FAMOUS COOKIES; NET WT. 7 OZ .(198g) BOX; BYRD COOKIE COMPANY 6700 WATERS SAVANNAH, GA…

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

Byrd Cookie Co.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 8, 2018

Drill (Fluted-Hard Bone), for Quattro Link 2.9mm, labeled as: a. Quattro Spade Drill, for 2.9mm, Model Number CM-9300;…

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

Cayenne Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

Diamedix Is-Mumps IgG Enzyme Immunoassay Test Kit for In Vitro Diagnostic Use Catalog No. 720-540

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

Diamedix Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 8, 2018

Ruffles Original potato chips 9 oz. bags

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

Frito-Lay, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 8, 2018

1) ELITE HV, Hemostasis Valve Introducer System, Sterile EO, Rx Only, Catalog #: a) BCL-100-04; b) BCL-100-05; c)…

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

Galt Medical Corporation

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

MAYFIELD INFINITY XR2 BASE UNIT, Part Number A2079 The MAYFIELD¿ Infinity XR2 Base Unit is intended to be used to…

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

Integra LifeSciences Corp.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 8, 2018

Kauffman's Fruit Farm & Market Sweet Apple Cider; Keep Refrigerated; Kauffman's Fruit Farm, Bird-in-Hand, PA 17505;…

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

Kauffman's Fruit Farm and Market, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 8, 2018

VNS Therapy Programming System, Rx Only, Model 3000, v1.0.2.2

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

XLTEK EMU40EX EEG Headbox

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

Natus Neurology dba Excel Tech., Ltd. (XLTEK)

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

Nicolet¿ Ambulatory EEG

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

Natus Neurology Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 8, 2018

Food Lion Dill Pickle Flavored Potato Chips 7.75 oz. package bag/12 bags per case

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

Shearer's Snacks

FDA (openFDA food enforcement)

Medical devices

Reported Aug 1, 2018

AD-TECH Medical Instrument Corporation Drill Sleeve Guides DSG-6-3-090-2.4N utilizing raw material (RM0677) from the…

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

Ad-Tech Medical Instrument Corporation

FDA (openFDA device enforcement)

Food

Reported Aug 1, 2018

AMPI Whey Powder, Sweet Type, Formula 521, Extra Grade, spray process pasteurized, packaged in 50 lbs net (22.68 kg…

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

Ampi

FDA (openFDA food enforcement)

Medical devices

Reported Aug 1, 2018

Arctic Sun Temperature Management System, Model 5000. The Arctic Sun¿ 5000 model is a non-invasive, thermal regulating…

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

Bard Medical Division

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

PR4100 Microplate Reader US, Catalog Number 45591587 Product Usage: The PR4100 Microplate Reader is a 96 well…

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

Bio-Rad Laboratories Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

Brivo XR385, model 5215463, Digital Diagnostic Radiographic System

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

MR Surgical Suite Option Product The MR Surgical Option when integrated with the GE Signa¿ 3.0T or 1.5T magnetic…

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

GE Medical Systems, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

ImplantDirect, Dental implants intended for use in partially and fully edentulous upper and lower jaws in support of…

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

Implant Direct Sybron Manufacturing, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

Leica Microsystems products labeled as the following: Leica M320 Microscope Systems with Article Numbers 10448419,…

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

Leica Microsystems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

Gibco CTS OpTmizer T Cell Expansion Serum Free Medium, bag format, Model Numbers A1048503 and A1022103. Tissue and cell…

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

Life Technologies, Corp.

5 more products in this recall

FDA (openFDA device enforcement)

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Other states

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.