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 5042150440 of 55,602 recalls

DrugJune 21, 2013· Tween Brands Inc

Recalled Item: Lemon anti bac Justice Recalled by Tween Brands Inc Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: LIFE IS SWEET! Justice Recalled by Tween Brands Inc Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: Grapefruit anti bac Justice Recalled by Tween Brands Inc Due to Labeling:...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: yum yum bubble gum Justice Recalled by Tween Brands Inc Due to Labeling:...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: Believe in Yourself Strawberry Anti bac Justice Recalled by Tween Brands Inc...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: I LOVE BACON Justice Recalled by Tween Brands Inc Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: FOLLOW YOUR DREAMS! Justice Recalled by Tween Brands Inc Due to Labeling:...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Bracco Diagnostics Inc

Recalled Item: Gastrografin (Diatrizoate Meglumine and Diatrizoate Sodium Solution)...

The Issue: Presence of foreign substance: One lot of the product may contain black...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 21, 2013· Price Chopper Golub Corperisable Warehouse

Recalled Item: Jacqueline's GOURMET COOKIES Brownie Burst Cookies Recalled by Price Chopper...

The Issue: Undeclared Milk allergen

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 21, 2013· Price Chopper Golub Corperisable Warehouse

Recalled Item: Jacqueline's GOURMET COOKIES Raspberry Burst Cookies Recalled by Price...

The Issue: Undeclared Milk allergen

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 21, 2013· Price Chopper Golub Corperisable Warehouse

Recalled Item: Jacqueline's GOURMET COOKIES Almond Bursts COOKIES Recalled by Price Chopper...

The Issue: Undeclared Milk allergen

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 20, 2013· Haemonetics Corporation

Recalled Item: TEG 5000 Thromboelastograph Coagulation Analyzer Product Usage: Multipurpose...

The Issue: Research Use Only (RUO) parameters were included in TEG 5000 User Manual.

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

Class II — Potential Health HazardOngoing
FoodJune 20, 2013· Beta Labs

Recalled Item: PHEnFX (TM) Recalled by Beta Labs Due to The products contain DMAA, also...

The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 20, 2013· Beta Labs

Recalled Item: RED VIPERS Recalled by Beta Labs Due to The products contain DMAA, also...

The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 20, 2013· Beta Labs

Recalled Item: Oxyphen XR Recalled by Beta Labs Due to The products contain DMAA, also...

The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 20, 2013· Beta Labs

Recalled Item: PHENTALENE (TM) Recalled by Beta Labs Due to The products contain DMAA, also...

The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 19, 2013· Philips Healthcare Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Healthcare...

The Issue: The MRx may deliver a non-synchronized cardioversion shock resulting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2013· Zimmer, Inc.

Recalled Item: VERSA-FX II FEMORAL FIXATION SYSTEM COMPRESSION TUBE/PLATE Recalled by...

The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2013· Zimmer, Inc.

Recalled Item: Free Lock Femoral Hip Fixation System Compression Lag Screw . Recalled by...

The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2013· Carestream Health Inc.

Recalled Item: DRX Revolution Recalled by Carestream Health Inc. Due to Carestream Health...

The Issue: Carestream Health Inc. is conducting a recall for the Column end Cover...

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

Class II — Potential Health HazardOngoing