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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 48,132 notices were distributed nationwide, so they reach Pennsylvania too — those are in the archive.

Medical devices

Reported Dec 31, 2014

KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 7.0 mm, Distributed by Kimberly Clark Global Sales, LLC.…

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

Halyard Health

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 31, 2014

ADULT Radiotransparent Electrode, Part number C100-PHILIPS, Rx ONLY, For use with Philips HeartStart AED "Comparable to…

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

Heart Sync, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 31, 2014

adaPT insight (12C), v1.3.2, PAT.109 (US), Treatment room 4: I2C is used with a charged particle or photon radiation…

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

Ion Beam Applications S.A.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 31, 2014

DPM 6 Patient Monitor and DPM 7 Patient Monitor. The product affected is the Mindray IBP module, P/N is 6800-30-50485…

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

Mindray DS USA, Inc. dba Mindray North America

FDA (openFDA device enforcement)

Medical devices

Reported Dec 31, 2014

Persona Cemented Tibial Broach Inserter/Extractor. The Persona Cemented Tibial Broach Inserter/Extractor Handle is a…

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

Zimmer, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 24, 2014

Farmer Brand DRIED LILY FLOWERS, NET WT. 8 oz, UPC 7 34765 04089 5 -- PRODUCT OF CHINA -- DISTRIBUTED BY BLOOMING…

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

Blooming Import Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 24, 2014

Innova IGS 540 Indicated for use for patients from newborn to geriatric in generating fluoroscopic and rotational…

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

GE Healthcare, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 24, 2014

GE Cabinet X-ray systems

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

GE Inspection Technologies, LP

FDA (openFDA device enforcement)

Food

Reported Dec 24, 2014

Dark Cocoa Sorbetto packed in 14 oz. plastic jars, 8 packages per case, manufactured from 4/11/14-4/12/14; product…

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

House Of Flavors, Inc.

FDA (openFDA food enforcement)

Food

Reported Dec 24, 2014

KOZY SHACK SIMPLY WELL CHOCOLATE, NET WT 4 OZ. Product packed in brown carton box, 48 individual units x 4 OZ. Keep…

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

Kozy Shack Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 24, 2014

RESTORIS PST Straight Shell Inserter An impactor is a reusable instrument designed for use by orthopedic surgeons…

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

Mako Surgical Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 24, 2014

SOLGAR ENHANCED SERIES ABC DOPHILUS POWDER FOR INFANTS AND CHILDREN, NET WT. 1.75 oz (50 g), UPC 0 33984 00010 0.…

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

NBTY, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 24, 2014

Additional devices identified in new FSN MA-FCO 83000190: QLAB versions 10.0 with a2DQ and/or aCMQ plug-ins installed…

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

Philips Ultrasound, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 24, 2014

Specialty Audible Torque Wrench Mfg by: Stryker Spine, Catalog number IS3002XLP, Non-sterile. Used to final tighten to…

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

Stryker Spine

FDA (openFDA device enforcement)

Food

Reported Dec 24, 2014

Wegmans Peach Salsa, made fresh in-store and packaged in random weights.

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

Wegmans Food Markets, Inc.

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 17, 2014

Total Temporomandibular Joint Replacement System- 45mm Lft Narrow Ti Mand

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

Biomet Microfixation, LLC

13 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 17, 2014

Distal Access Catheter: Model Numbers: 90121, 90130, 90131, 90160. The Distal Access Catheter is intended for use in…

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

Concentric Medical Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 17, 2014

INOMAX DSIR Nitric Oxide delivery system, Model 10007, software version 3.1.0., delivers INOMAX (nitric oxide for…

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

INO Therapeutics (dba Ikaria)

FDA (openFDA device enforcement)

Medical devices

Reported Dec 17, 2014

A uterine tenaculum is a hook-like instrument used to seize and hold the cervix or fundus sold under the CareFusion,…

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

Instrumed International, Inc.

27 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 17, 2014

Invacare Perfecto 2 V Oxygen Concentrator The finished device is packaged as a single unit. The service part contains a…

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

Invacare Corporation

FDA (openFDA device enforcement)

Food

Reported Dec 17, 2014

Chicken flavored broth base and seasoning, low sodium sold under the Orrington Farms brand in 5 oz. plastic jars.

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

Kent Precision Foods Group, Inc.

FDA (openFDA food enforcement)

Food

Reported Dec 17, 2014

Margaret Holmes Mixed Greens 14.5 oz, Distributed by McCall Farms, Effingham, SC

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

Mccall Farms Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 17, 2014

ESSENTIA Hydration Perfected Purified Water and Electrolytes, 9.5 pH, Manufactured for Essentia Water Inc., 22833…

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

Nature's Way Purewater Systems, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 17, 2014

Covidien Puritan Bennett 980 Ventilator, Rx ONLY, Made in Ireland., Covidien LLC, USA. REF 980X1ENDIUU.

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

Nellcor Puritan Bennett Inc. (dba Covidien LP)

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.