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. 2,919 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,919 in last 12 months

Showing 921940 of 55,602 recalls

Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX450. Product Number: 866062. Recalled by...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue MP70. Product Number: M8007A. Recalled by Philips North America...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Stryker Corporation

Recalled Item: NICO BrainPath Recalled by Stryker Corporation Due to Tape used to secure...

The Issue: Tape used to secure components within packaging contains latex, despite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Stryker Corporation

Recalled Item: NICO Myriad Handpiece Product Number/Product Name: NN-8000 15x10 MHP...

The Issue: Tape used to secure components within packaging contains latex, despite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Stryker Corporation

Recalled Item: NICO Myriad Illumination Pack Product No. NN-1000 11g Illumination...

The Issue: Tape used to secure components within packaging contains latex, despite...

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

Class II — Potential Health HazardOngoing
FoodOctober 30, 2025· Lotus Vaping Technologies, LLC

Recalled Item: Monarch Premium Kratom Green Maeng Da powder is packaged in Recalled by...

The Issue: Product has the potential to be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 30, 2025· Lotus Vaping Technologies, LLC

Recalled Item: Monarch Premium Kratom White Elephant powder is packaged in seal Recalled by...

The Issue: Product has the potential to be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 30, 2025· Lotus Vaping Technologies, LLC

Recalled Item: Monarch Premium Kratom Red Bali powder is packaged in seal Recalled by Lotus...

The Issue: Product has the potential to be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 30, 2025· Lotus Vaping Technologies, LLC

Recalled Item: Monarch Premium Kratom Bali Gold powder is packaged in seal Recalled by...

The Issue: Product has the potential to be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 30, 2025· Cepheid

Recalled Item: Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-10 Recalled...

The Issue: Invitro diagnostic test kits with specimens that have elevated white blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2025· Cepheid

Recalled Item: Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-US-10...

The Issue: Invitro diagnostic test kits with specimens that have elevated white blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Medicrea International

Recalled Item: Medicrea Recalled by Medicrea International Due to Due to complaints,...

The Issue: Due to complaints, orthopedic rotation tool handle may untread from the...

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

Class II — Potential Health HazardOngoing
FoodOctober 29, 2025· Avion Pharmaceuticals, LLC

Recalled Item: Prenate Chewable¿ A chewable Rx prenatal vitamin with a delicious Recalled...

The Issue: Undeclared Soy. The firm received positive test results for soy which is not...

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

Class III — Low RiskOngoing
Refund
DrugOctober 29, 2025· Otsuka ICU Medical LLC

Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by Otsuka ICU Medical LLC Due to Labeling:...

The Issue: Labeling: Label Error on Declared Strength-The overwrap label may...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 29, 2025· Otsuka ICU Medical LLC

Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by Otsuka ICU Medical LLC Due to Labeling:...

The Issue: Labeling: Label Error on Declared Strength-The overwrap label may...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 29, 2025· Medicrea International

Recalled Item: Medicrea Recalled by Medicrea International Due to Due to complaints,...

The Issue: Due to complaints, orthopedic rotation tool handle may untread from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Copan Italia

Recalled Item: 1ml of DTT in liquid phase Recalled by Copan Italia Due to Treatment reagent...

The Issue: Treatment reagent functionality in respiratory specimens liquification...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Copan Italia

Recalled Item: 1ml of DTT in liquid phase Recalled by Copan Italia Due to Treatment reagent...

The Issue: Treatment reagent functionality in respiratory specimens fluidification...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Philips North America Llc

Recalled Item: CT 5300 Recalled by Philips North America Llc Due to If the screws of tube...

The Issue: If the screws of tube heat exchanger on the rotating scanner are not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Philips North America Llc

Recalled Item: Incisive CT Recalled by Philips North America Llc Due to If the screws of...

The Issue: If the screws of tube heat exchanger on the rotating scanner are not...

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

Class II — Potential Health HazardOngoing