Product Recalls in Pennsylvania

Product recalls affecting Pennsylvania — including food, drugs, consumer products, medical devices, and vehicles distributed to Pennsylvania. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,064 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
1,064 in last 12 months

Showing 21401–21420 of 55,602 recalls

Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Luminos Agile Max Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A software bug may lead to one image to be assigned to two different...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Ysio Max Recalled by Siemens Medical Solutions USA, Inc Due to A software...

The Issue: A software bug may lead to one image to be assigned to two different...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodJanuary 8, 2020· Healthy Food Ingredients, LLC

Recalled Item: Organic IntegriPure Cold Milled Flaxseed Recalled by Healthy Food...

The Issue: Product is being recalled due to detection of an unapproved herbicide.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Healthineers Luminos dRF Max Model: 10762471- Product Usage: is...

The Issue: Two software issues (1) Using the override function in case of blocked...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Healthineers Luminos Agile Max Model: 10762472 - Product Usage:...

The Issue: Two software issues (1) Using the override function in case of blocked...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Healthineers Uroskop Omnia max Model: 10762473 - Product Usage:...

The Issue: Two software issues (1) Using the override function in case of blocked...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Healthineers Ysio Max - Interventional Fluoroscopic X-Ray System...

The Issue: Two software issues (1) Using the override function in case of blocked...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Care Essentials Pty., Ltd.

Recalled Item: Cocoon Convective Warming System Recalled by Care Essentials Pty., Ltd. Due...

The Issue: Potential for thermal damage near the power cord connector and Power Entry...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Zimmer Biomet, Inc.

Recalled Item: THP Hip Plating System Recalled by Zimmer Biomet, Inc. Due to Potential...

The Issue: Potential increase in fracture rate was detected during internal testing, in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Care Essentials Pty., Ltd.

Recalled Item: Cocoon Convective Warming System Recalled by Care Essentials Pty., Ltd. Due...

The Issue: Potential for thermal damage near the power cord connector and Power Entry...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Smiths Medical ASD, Inc.

Recalled Item: Portex LineDraw Arterial Blood Sampling Syringe with Dry Lithium Heparin...

The Issue: Portex Pro-Vent and LineDraw Arterial Blood Sampling syringes may have...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Smiths Medical ASD, Inc.

Recalled Item: Portex ProVent Arterial Blood Sampling Kit with Dry Lithium Heparin Recalled...

The Issue: Lots of Smiths Medical Portex Pro-Vent and LineDraw Arterial Blood Sampling...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Stryker Corporation

Recalled Item: Spy-Phi Drape only (HH2020) Pack of 20 HH2000 (Sold internationally Recalled...

The Issue: Sterile drapes packaged in an unsealed pouch.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Palodex Group Oy

Recalled Item: KaVo Scan eXam SOLID STATE X-RAY IMAGER (FLAT PANEL/DIGITAL IMAGER) Recalled...

The Issue: Slow degradation of plastic insulation used in the PSU DC plug of the DIGORA...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Palodex Group Oy

Recalled Item: Soredex DIGORA Optime SOLID STATE X-RAY IMAGER (FLAT PANEL/DIGITAL IMAGER)...

The Issue: Slow degradation of plastic insulation used in the PSU DC plug of the DIGORA...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Palodex Group Oy

Recalled Item: Gendex GXPS-500 SOLID STATE X-RAY IMAGER (FLAT PANEL/DIGITAL IMAGER)...

The Issue: Slow degradation of plastic insulation used in the PSU DC plug of the DIGORA...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Palodex Group Oy

Recalled Item: Instrumentarium Dental Express SOLID STATE X-RAY IMAGER (FLAT PANEL/DIGITAL...

The Issue: Slow degradation of plastic insulation used in the PSU DC plug of the DIGORA...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· CME America, LLC

Recalled Item: CME America BodyGuard Infusion Pump System Recalled by CME America, LLC Due...

The Issue: Infusion Pump Systems may have a delivery inaccuracy of up to 13%, which may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 7, 2020· Stryker Corporation

Recalled Item: Spy-Phi Drape (HH2000) sold as a Spy-Phi Pack (HH9006). Only Recalled by...

The Issue: Sterile drapes packaged in an unsealed pouch.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJanuary 7, 2020· AVKARE Inc.

Recalled Item: Dutasteride Capsules Recalled by AVKARE Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund