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. 1,818 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
1,818 in last 12 months

Showing 4686146880 of 55,602 recalls

Medical DeviceMay 6, 2014· Advanced Photonic Systems, LLC

Recalled Item: Photonica Light Modulator. These include all products labeled as UltraSlim...

The Issue: Marketing without marketing clearance or approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens LANTIS System Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: There is a potential risk when using LANTIS OIS System client software with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2014· Beaver-Visitec International Inc.

Recalled Item: Visitec Anterior Chamber Cannula Recalled by Beaver-Visitec International...

The Issue: Contains a sharp tip needle when the product should contain a blunt tip cannula

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

Class II — Potential Health HazardOngoing
DrugMay 5, 2014· Eugene Oregon, Inc.

Recalled Item: AFRICAN BLACK ANT Recalled by Eugene Oregon, Inc. Due to Undeclared Sildenafil

The Issue: Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 5, 2014· Eugene Oregon, Inc.

Recalled Item: MOJO RISEN Recalled by Eugene Oregon, Inc. Due to Undeclared Sildenafil

The Issue: Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 5, 2014· Eugene Oregon, Inc.

Recalled Item: Black Ant Recalled by Eugene Oregon, Inc. Due to Undeclared Sildenafil

The Issue: Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 5, 2014· Axcentria Pharmaceuticals, LLC

Recalled Item: Hemo-Stat Solution Recalled by Axcentria Pharmaceuticals, LLC Due to...

The Issue: Marketed without an Approved NDA/ANDA; product is being manufactured and...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 5, 2014· Philips Medical Systems, Inc.

Recalled Item: All Philips Ingenia Recalled by Philips Medical Systems, Inc. Due to In...

The Issue: In spine clinical workflows, cross lines may be used to determine the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2014· Mckesson Medical Immaging

Recalled Item: Horizon Medical Imaging It is a medical image and information Recalled by...

The Issue: The firm has identified a software issue which may cause a discrepancy...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2014· DIABETIC SUPPLY OF SUNCOAST, INC.

Recalled Item: ADVOCATE Redi-Code+ BMB-BA006A Blood Glucose test strips Product Usage: The...

The Issue: "Advocate Redi-Code + BMB-BA006A Blood Glucose test strips" are...

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

Class I — Serious Health HazardOngoing
DrugMay 2, 2014· Fresenius Kabi USA, LLC

Recalled Item: Fosphenytoin Sodium Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Presence of Particular Matter: Potential glass delamination and consistent...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 2, 2014· Fresenius Kabi USA, LLC

Recalled Item: Fosphenytoin Sodium Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Presence of Particular Matter: Potential glass delamination and consistent...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 2, 2014· Bazzini Holdings L.L.C.

Recalled Item: Barricini Milk Chocolate Peanut Butter Pretzels in Net Wt 6.5 oz. plastic...

The Issue: Undeclared wheat. The back panel applied to some containers of milk...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 2, 2014· Anhing Corporation

Recalled Item: Caravelle CHILI POWDER HOT Net Weight 8 oz. (227G) Recalled by Anhing...

The Issue: Anhing Corporation is recalling Caravelle Brand Chili Powder because it has...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 2, 2014· Alere San Diego, Inc.

Recalled Item: Alere Triage¿ D-Dimer Test PN 98100 Recalled by Alere San Diego, Inc. Due to...

The Issue: Alere initiated this recall because a limited number of Alere Triage¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2014· GE Healthcare, LLC

Recalled Item: Kenex Radiation Shield and surgical lamps installed with GE Healthcare...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to...

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

Class II — Potential Health HazardOngoing
DrugMay 1, 2014· Boehringer Ingelheim Roxane Inc

Recalled Item: Calcitriol Oral Solution 1 mcg/mL Recalled by Boehringer Ingelheim Roxane...

The Issue: Failed Impurity/Degradation Specification; out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 1, 2014· Teva Pharmaceuticals USA

Recalled Item: Dextroamphetamine Sulfate Tablets Recalled by Teva Pharmaceuticals USA Due...

The Issue: Failed Impurities/Degradation Specifications: this product is being recalled...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 1, 2014· Pepsi Beverages Company

Recalled Item: Lipton Pure Leaf Iced Tea Lemon 18.5OZ PL 12 Pack Recalled by Pepsi...

The Issue: Pepsi Co has announced a recall of some Lipton Pure Leaf Iced Tea products...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 1, 2014· Pepsi Beverages Company

Recalled Item: Lipton Pure Leaf Iced NTS Honey Green Tea 12 Pack Recalled by Pepsi...

The Issue: Pepsi Co has announced a recall of some Lipton Pure Leaf Iced Tea products...

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

Class II — Potential Health HazardOngoing
Refund