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 48,828 notices were distributed nationwide, so they reach Pennsylvania too — those are in the archive.

Food

Reported Jun 19, 2019

Park Street Deli, Hummus and Veggies, Classic Hummus, Carrots & Celery NET WT 5 OZ (142g)

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

Del Monte Fresh Produce N.A., Inc. HQ

FDA (openFDA food enforcement)

Medical devices

Reported Jun 19, 2019

IntraClude Intra-Aortic Occlusion Device, REF: ICF100, 10.5 Fr (3.5 mm) X 39.4" (100 cm), Rx Only, Sterile EO The…

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 19, 2019

Prestige II, Prestige SI, Prestige VH Prestige system is a new multi-purpose conventional and digital R/F remote…

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

GE Healthcare, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 19, 2019

Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86662003 Product Usage: Usage: The Getinge 86 Series…

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

Maquet Cardiovascular US Sales, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

MRSASelect, IVD, REF 63747, containing 20 plates per package. The MRSASelect is indicated for use in conjunction with…

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

Bio-Rad Laboratories, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution

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

Kerr/Pentron, dba Kerr Corporation and Pentron Clinical

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

Leica Cryostats, used to produce frozen sample sections for biological, medical and industrial applications, including…

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

Leica Microsystems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

Cepheid Xpert MRSA/MRSA NxG Control Panel (Catalog #8195) UDI: 70845357041226 Product Usage: On April 9, 2019,…

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

Microbiologics Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

NxStage PureFlow B Solution, REF RFP-400, M535RFP4000 Product NxStage PureFlow B Solution is indicated for use with…

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

NxStage Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV16F

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

OriGen Biomedical, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

Portex Blue Line Ultra Tracheostomy Tube Inner Cannula. One cannula comes inside a package which is labeled in part,…

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

Smiths Medical ASD Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 12, 2019

Strawberry Banana Smoothie, 3.1oz, 6 pack, UPC Code 52159-70082

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

Stonyfield Farm

FDA (openFDA food enforcement)

Medical devices

Reported Jun 12, 2019

Stryker Neurovascular, AXS Infinity LS Plus Long Sheath, Rx Only, Sterile EO, USA Customer Service 855-91 NEURO…

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

Stryker Neurovascular

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2019

Abbott MitraClip XTR Clip Delivery System, UDI: 08717648226366, Part: CDS0601-XTR, Sterile EO, Rx Only

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

Abbott Vascular

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2019

Horizon Cardiology Hemo

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

Change Healthcare Israel Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 5, 2019

Dole Classic Coleslaw (US) Shredded cabbage and carrots. 14 oz. US

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

Dole Fresh Vegetables

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Jun 5, 2019

Fiddyment Farms Fiddy Fire In-Shell Pistachios 2.5 oz., 8 oz., 1 lb., 2 lb., 3 lb., 5 lb., Fiddyment Farms Fiddy Fire…

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

Fiddyment Farms Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 5, 2019

Fenestrated Taps 4.5mm, 5.5mm, 6.5mm (Ref#5001-90013, 5001-90014, 5001-90015) Product Usage: The K2M Fenestrated Tap…

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

K2M, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2019

King LTS-D Kit Size 1, Model Number KLTSD431

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

King Systems Corp. dba Ambu, Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 5, 2019

Suja Organic Kombucha - Ginger Lemon: 15.2 oz. glass bottle; UPC 818617020232 DISTRIBUTED BY SUJA LIFE, LLC OCEANSIDE,…

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

Suja Life LLC

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported May 29, 2019

Trader Joe s Vegetable Melange In Seasoned Butter Sauce Packed in 16 ounce plastic packages retail packaging Bar code:…

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

Ardo N.V.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 29, 2019

EV1000 Clinical Platform, Models: EV1000A, EV1000NI, EV1000CS Product Usage: EV1000A Monitor is used to optimize fluid…

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2019

Leksell GammaPlan 11.1 Product Usage: Leksell GammaPlan is a computer-based system designed for Leksell Gamma Knife…

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

Elekta Instrument AB

FDA (openFDA device enforcement)

Drugs

Reported May 29, 2019

Losartan Potassium Tablets USP 25 mg 30 count bottle NDC 60429-316-30 Rx only GSMS Incorporated

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

Golden State Medical Supply Inc.

4 more products in this recall

FDA (openFDA drug 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.