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. 2,863 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,863 in last 12 months

Showing 93219340 of 55,602 recalls

FoodJune 9, 2023· Richin Trading Inc

Recalled Item: Sun Wave Brand Jelly Cup (Lychee Flavor) Recalled by Richin Trading Inc Due...

The Issue: Potential choking hazard

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 9, 2023· Richin Trading Inc

Recalled Item: Sun Wave Brand Jelly Cup (Mango Flavor) Recalled by Richin Trading Inc Due...

The Issue: Potential choking hazard

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 9, 2023· Richin Trading Inc

Recalled Item: Sun Wave Brand Jelly Cup (Assorted Flavors) Recalled by Richin Trading Inc...

The Issue: Potential choking hazard

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 8, 2023· Olympus Corporation of the Americas

Recalled Item: HF Resection Electrodes - HF resection electrodes are part of Recalled by...

The Issue: Additional Caution statements in IFU: (1) Due to complaints where the loop...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2023· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices Recalled by Argon Medical Devices, Inc Due to There is...

The Issue: There is the potential that the vena Cava Filter may not perform as intended...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus BRONCHOFIBERSCOPE BF Type Recalled by Olympus Corporation of the...

The Issue: There have been complaints of endobronchial combustion during therapeutic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus EVIS EXERA III BRONCHOVIDEOSCOPE BF TYPE Recalled by Olympus...

The Issue: There have been complaints of endobronchial combustion during therapeutic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus BRONCHOVIDEOSCOPE Recalled by Olympus Corporation of the Americas...

The Issue: There have been complaints of endobronchial combustion during therapeutic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus EVIS EXERA BRONCHOVIDEOSCOPE BF TYPE Recalled by Olympus Corporation...

The Issue: There have been complaints of endobronchial combustion during therapeutic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus OES BRONCHOFIBERSCOPE BF Type Recalled by Olympus Corporation of the...

The Issue: There have been complaints of endobronchial combustion during therapeutic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus BRONCHOVIDEOSCOPE BF Type Recalled by Olympus Corporation of the...

The Issue: There have been complaints of endobronchial combustion during therapeutic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus EVIS EXERA II BRONCHOVIDEOSCOPE BF TYPE Recalled by Olympus...

The Issue: There have been complaints of endobronchial combustion during therapeutic...

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

Class I — Serious Health HazardOngoing
FoodJune 7, 2023· Oregon Potato Company

Recalled Item: Rader Farms Organic Fresh Start Smoothie Blueberry Recalled by Oregon Potato...

The Issue: Potential contamination with Hepatitis A.

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 7, 2023· Oregon Potato Company

Recalled Item: Great Value Sliced Strawberries. Item # 107356. Frozen Recalled by Oregon...

The Issue: Potential contamination with Hepatitis A.

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 7, 2023· Oregon Potato Company

Recalled Item: Great Value Mixed Fruit Pineapple Recalled by Oregon Potato Company Due to...

The Issue: Potential contamination with Hepatitis A.

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 7, 2023· Oregon Potato Company

Recalled Item: Rader Farms Organic Berry Trio Strawberry Recalled by Oregon Potato Company...

The Issue: Potential contamination with Hepatitis A.

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 7, 2023· Oregon Potato Company

Recalled Item: Great Value Antioxidant Fruit Blend Strawberries Recalled by Oregon Potato...

The Issue: Potential contamination with Hepatitis A.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 7, 2023· PTW-FREIBURG

Recalled Item: BeamAdjust software Version 2.3.3 The following devices are Recalled by...

The Issue: Generated calibration file will not be correct in case of a relative...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2023· MICROVENTION INC.

Recalled Item: FRED Flow Re-Direction Endoluminal Device Recalled by MICROVENTION INC. Due...

The Issue: Intracranial aneurysm flow diverter device may be manufactured with an...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2023· Murata Vios, Inc.

Recalled Item: Vios Monitoring System Bedside Monitor Recalled by Murata Vios, Inc. Due to...

The Issue: A premature failure condition was identified with the L2050R pulse oximeter...

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

Class II — Potential Health HazardOngoing