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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 48,122 notices were distributed nationwide, so they reach Pennsylvania too — those are in the archive.

Medical devices

Reported Mar 7, 2018

ST AIA-PACK¿ PROG II, Progesterone II Assay, Part Number: 025239

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

Tosoh Bioscience Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 7, 2018

Camera System, Television, Surgical without audio Intended for transmission and documentation of surgical interventions…

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

Trumpf Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 7, 2018

Zimmer Segmental System, ZSS Distal Femur. Sizes as follows: a. Size B-LT (Item No. 00585001201); b. Size B-RT (Item…

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

Zimmer Biomet, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Mar 1, 2018

Sensenig Turkey Farm LLC Retira Productos De Salchicha De Pavo Debido A Un Error De Rotulacin Y Alrgenos No Declarados

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

Sensenig Turkey Farm LLC

USDA FSIS

Medical devices

Reported Feb 28, 2018

Innova Self-Expanding Stent System, 200 mm. Labeled with Material Number and description as follows: Product Usage: The…

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

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 28, 2018

Flexfrost Protein Ice Cream Chocolate Flexfrost L.L.C. 622 RT 10 Whippany, NJ 07981

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

Flexfrost

4 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 28, 2018

Frozen Unbaked Biscuits sold under the brand names of Hilltop Hearth, Mary B's & Marshall.

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

Holsum Baking Company Warehouse

FDA (openFDA food enforcement)

Medical devices

Reported Feb 28, 2018

Pentax Video Duodenoscope Model: ED-3490TK (UDI of design being recalled: 04961333232420) These instruments are…

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

Pentax

FDA (openFDA device enforcement)

Medical devices

Reported Feb 28, 2018

Cobas 8000 Modular Series system; Software Version 05-02 and 06-03; UDI: 05641446001

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

Roche Diagnostics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 28, 2018

ROSA Brain 3.0 Stereotaxic instrument Computer-assisted surgical device. Intended for the spatial positioning and…

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

Zimmer Biomet, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 21, 2018

Arthri-D 120ct

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

ABH Nature's Products, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 21, 2018

AVID Medical QA Pack AV10654-10

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

Avid Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2018

Lyophilized Chemistry Calibrator Level 1 Product Usage: Beckman Coulter Chemistry Calibrators are intended for use when…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 21, 2018

WALNUT CREEK FOODS Caramel Popcorn NET WT 15 OZ (425g) Ingredients: Evaporated Can Juice, Popcorn, Butter (cream,…

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

Coblentz Distributing Inc. dba Walnut Creek Foods

FDA (openFDA food enforcement)

Medical devices

Reported Feb 21, 2018

Central Venous Catheter Set Triple Lumen Polyurethane, Catalog Identifier: C-UTLM-501J Product Usage: The central…

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

Cook Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2018

Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1

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

GE Medical Systems China Co., Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 21, 2018

Frozen Sliced (blanched) Squash packed in 1400 lb. plastic totes.

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

Hanover Foods Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Feb 21, 2018

Vado Steerable Sheath 8.8F, REF SS8FMU67, packaged in a lidded tray that is within a pouch which is inserted into a…

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

Kalila Medical

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 21, 2018

Live Better Drug Free Black Elderberry Syrup, 4 FL OZ (118 mL); DIETARY SUPPLEMENT, UPC 050428581186

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

Kingston Pharma LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 21, 2018

Ingenuity TF PET/CT (model 882442) running software version 4.0.2 This device is a diagnostic imaging system that…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 21, 2018

STAR WARS TIN WITH CARAMEL POPCORN NET WT 3.5 oz (99g) CONTAINS MILK AND SOY, MAY CONTAIN TREE NUTS AND PEANUTS…

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

Ross Acquisitions Company

FDA (openFDA food enforcement)

Medical devices

Reported Feb 21, 2018

Artis oneFloor-mounted system for uncompromised imaging; Artis one, Interventional fluoroscopic x-ray system, Artis one…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2018

11MM/130 Degree Titanium Trochanteric Fixation Nail 380MM/Right, Sterile

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

Synthes (USA) Products LLC

FDA (openFDA device enforcement)

Food

Reported Feb 21, 2018

Weis Weis Markets, Inc., Sunbury, PA 17801-0471; Keep Refrigerated; Dried Beef Party Rye Dip; Ingredients: Hellman's…

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

Weis Markets

FDA (openFDA food 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.