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 93019320 of 55,602 recalls

DrugJune 13, 2023· AVKARE LLC

Recalled Item: Tranexamic Acid USP Tablets Recalled by AVKARE LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 13, 2023· Randox Laboratories Ltd.

Recalled Item: Randox RX Series Urea Enzymatic Kinetic Assay Ref. Numbers: (1) Recalled by...

The Issue: Carryover from the Direct LDL-cholesterol assay on the Rx instruments may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2023· Medtronic Neurosurgery

Recalled Item: Durepair Dura Regeneration Matrix: DUREPAIR DURA SUBSTITUTE 2 X 2 Recalled...

The Issue: Dura regeneration matrix may have out-of-specification endotoxin levels due...

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

Class II — Potential Health HazardOngoing
DrugJune 12, 2023· Ferring Pharmaceuticals Inc

Recalled Item: Endometrin (progesterone) Vaginal Insert 100mg Recalled by Ferring...

The Issue: cGMP deviations: potential for Microbial Contamination of Non-Sterile Products

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2023· Amring Pharmaceuticals Inc

Recalled Item: Lysteda (tranexamic acid) USP Tablets Recalled by Amring Pharmaceuticals Inc...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class III — Low RiskOngoing
Refund
FoodJune 12, 2023· Wow Factor Desserts

Recalled Item: WOW! Factor Desserts Berry Burst Slab Cake. Weight 2x8.15lbs Recalled by Wow...

The Issue: Possible norovirus contamination

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 12, 2023· Supplement Manufacturing Partner, Inc.

Recalled Item: Havasu Beetroot Powder Recalled by Supplement Manufacturing Partner, Inc....

The Issue: Contains undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 12, 2023· Philips North America

Recalled Item: Ingenia Elition X Magnetic Resonance (MR) system Recalled by Philips North...

The Issue: During installation of the SmokeDetector Interlock, a connecting cable,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2023· Philips North America

Recalled Item: MR 7700 Magnetic Resonance (MR) system Recalled by Philips North America Due...

The Issue: During installation of the SmokeDetector Interlock, a connecting cable,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2023· Philips North America

Recalled Item: Ingenia Elition X Magnetic Resonance (MR) system Recalled by Philips North...

The Issue: The system operator is able to bypass the SmokeDetector Interlock system...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2023· Philips North America

Recalled Item: MR 7700 Magnetic Resonance (MR) system Recalled by Philips North America Due...

The Issue: The system operator is able to bypass the SmokeDetector Interlock system...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2023· Philips North America

Recalled Item: Ingenia Elition S Magnetic Resonance (MR) system Recalled by Philips North...

The Issue: The system operator is able to bypass the SmokeDetector Interlock system...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2023· Philips North America

Recalled Item: Ingenia Elition S Magnetic Resonance (MR) system Recalled by Philips North...

The Issue: During installation of the SmokeDetector Interlock, a connecting cable,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2023· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 7 M20. X-ray Image guided Therapy System. Recalled by PHILIPS...

The Issue: The bolts supporting the FlexMove Carriage may become loose and/or break,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2023· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10 and FD20. X-ray Imaging System. Recalled by PHILIPS MEDICAL...

The Issue: The bolts supporting the FlexMove Carriage may become loose and/or break,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2023· Draeger Medical, Inc.

Recalled Item: Oxylog 3000 Plus emergency and transport ventilator Recalled by Draeger...

The Issue: Draeger has become aware of instances where the device stopped working when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 12, 2023· Abbott

Recalled Item: Abbott Amplatzer Steerable Delivery Sheath (ASDS) Recalled by Abbott Due to...

The Issue: There is an overall reported incidence rate of 0.77% related to observed or...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 12, 2023· Intuitive Surgical, Inc.

Recalled Item: da Vinci Xi/X Tip-Up Fenestrated Grasper Recalled by Intuitive Surgical,...

The Issue: Fenestrated Graspers have a manufacturing issue has the potential to cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2023· Tornier, Inc

Recalled Item: AEQUALIS FLEX REVIVE Assembly Screw 0mm Short Recalled by Tornier, Inc Due...

The Issue: A comingle/swap resulted in the labeling and laser marking on the product to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2023· Tornier, Inc

Recalled Item: AEQUALIS FLEX REVIVE Assembly Screw 0mm Recalled by Tornier, Inc Due to A...

The Issue: A comingle/swap resulted in the labeling and laser marking on the product to...

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

Class II — Potential Health HazardOngoing