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

Medical devices

Reported Nov 18, 2015

MILEX PESSARY KIT; Model Numbers: MXPES00; MXKPES00; MXKPREG03; MXKPGSK07 Product Usage: The Coopersurgical MILEX…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2015

Ventilator Tubing

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

Instrumentation Industries Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2015

Stryker Orthopaedics, MIS MODULAR DISTAL CAPTURE TRIATHLON MIS INSTRUMENTS, REF 6541-5-723, Lot AdminECR19205,…

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

Stryker Howmedica Osteonics Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2015

Stryker Radius 5.5 to 3.5 Rod to Red Connector, REF 48664530. Intended to provide additional support during fusion…

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

Stryker Spine

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2015

SSS Reprocessed Zimmer, Synthes, Stryker and Linvatec Drill Bits and Blades Surgical drill bits, blades, burs, chisels,…

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

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2015

Synthes Small Notch Titanium Reconstructive Plate set (SNTRP). Ti PLATE/ROD/PLATE 231mm 6HOLES/5.0mm ROD/17HOLES.…

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

Synthes (USA) Products LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2015

Myelo-Nate CSF Sampling Kit, Neonatal/Pediatric cerebralspinal fluid sampling sterile tray, including a lumbar puncture…

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

Utah Medical Products, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2015

Triton Infusion Pump (model 300000) and Triton fp Infusion Pump (model 400000) (proprietary name: AFF (Mark I)…

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

WalkMed Infusion, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 11, 2015

ARROW PICC Kit featuring Chlorag+ard Technology Midline Catheterization Kit ARROW Advantage5 Pressure Injectable PICC…

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

Arrow International Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 11, 2015

Antibacterial Hydro Personal Catheter, Male 12 Fr, Product Code 63512, sold in boxes of 30 units

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

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 11, 2015

The Centricity PACS-IW with Universal Viewer is a device that displays medical images (including mammograms) and data…

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

GE Healthcare

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 11, 2015

Helioseal F Sealant Refill 1 x 1.25 g, REF 558519AN, and Helioseal F Assortment (kit) 5 x 1.25 g, REF 558518AN. Dental…

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

Ivoclar A. G.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 11, 2015

Robotic Arm Interactive Orthopedic (RIO) system component PN#205143 (locking pin) and PN# 112220 (connector). Indicated…

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

Mako Surgical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 11, 2015

Medtronic Achieve Cables, model 990066. The sterile, single use only Electrical Cable (Model 990066) provides the…

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

Medtronic Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 11, 2015

GEMINI PET/CT System, a diagnostic imaging system for fixed or mobile installations that combines Positron Emission…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 4, 2015

American Pure Whey, Whey Protein Matrix Chocolate flavor, 2 lb. and 5 lb. containers, Manufactured by American Pure…

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

American Pure Whey

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 4, 2015

BD CD3 (SK7) FITC; IVD; Catalog # 349201 and 340542 Hematology: The CD3 antibody reacts with the epsilon chain of the…

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

Becton, Dickinson and Company, BD Biosciences

FDA (openFDA device enforcement)

Food

Reported Nov 4, 2015

Sunkist Frozen Mango Fruit Sorbet Bar 6 x 2.5 FL OZ. (74 mL) Bars/ 15 FL OZ (444 mL) and pint (473 mL) UPC: 51819-00303

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

Dean Foods, Inc.

FDA (openFDA food enforcement)

Food

Reported Nov 4, 2015

Goya Mojo Criollo Marinade for Chicken, Pork & Beef (a) 12 ounce (b) 24.5 oz and (c) 1 Gallon containers; Goya Foods,…

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

Goya Foods

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 4, 2015

CC cartridges for IRMA TRUPOINT Blood Gas Analyzer, PN 039903. The CC Cartridge are single use, disposable, in vitro…

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

LifeHealth, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 4, 2015

Trader Joes Coconut Cranberry Granola (SKU 51131), packaged in a 16 oz. box, with Best By date 08/19/16 printed at…

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

New England Natural Bakers, Inc.

FDA (openFDA food enforcement)

Food

Reported Nov 4, 2015

Sobisk Lemon Cream Cookies; Imported Exclusively by: Sobisk Foods, LLC, 110 W Baltimore Ave, Clifton heights, PA 19018;…

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

Sobisk Foods LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 28, 2015

XiO Radiation Treatment Planning System. Used to create treatment plans for any cancer patient for whom external beam…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2015

AltiVate Humeral Socket Shell Trial, Part Number 804-06-052 The glenoid baseplate is intended for cementless…

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

Encore Medical, LP

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.