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 88018820 of 55,602 recalls

DrugAugust 9, 2023· Ecometics, Inc.

Recalled Item: YAGER'S LINIMENT (Camphor and Turpentine Oil) 3.1% and 8.12% respectively...

The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 9, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Proboscis/Piston Assembly Recalled by Ortho-Clinical Diagnostics, Inc. Due...

The Issue: Ortho Clinical Diagnostics (QuidelOrtho) confirmed certain Proboscis/Piston...

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

Class II — Potential Health HazardOngoing
FoodAugust 8, 2023· David Oppenheimer & Company I LLC

Recalled Item: Zespri Organic Green Kiwi Recalled by David Oppenheimer & Company I LLC Due...

The Issue: Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 8, 2023· David Oppenheimer & Company I LLC

Recalled Item: Zespri Organic Green Kiwi Recalled by David Oppenheimer & Company I LLC Due...

The Issue: Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 8, 2023· Real Kosher Ice Cream, Inc.

Recalled Item: Soft Serve on the Go brand Razzle n' Dazzle Peanut Butter flavor Recalled by...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 8, 2023· Real Kosher Ice Cream, Inc.

Recalled Item: Soft Serve on the Go brand Caramel Vanilla flavor Recalled by Real Kosher...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 8, 2023· Bickel's Snack Foods Inc

Recalled Item: Butter Flavored Popcorn Naturally & Artificially Flavored Recalled by...

The Issue: Undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 8, 2023· Real Kosher Ice Cream, Inc.

Recalled Item: Soft Serve on the Go brand Vanilla Chocolate flavor Recalled by Real Kosher...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 8, 2023· Real Kosher Ice Cream, Inc.

Recalled Item: Soft Zero on the Go brand Lite Peanut Butter flavor Recalled by Real Kosher...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 8, 2023· Real Kosher Ice Cream, Inc.

Recalled Item: Soft Serve on the Go brand Sorbet Strawberry Mango Sorbet flavor Recalled by...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 8, 2023· FX SHOULDER

Recalled Item: Centered Glenosphere w/Screw Recalled by FX SHOULDER Due to Centered...

The Issue: Centered glenosphere box may contain an eccentric glenosphere.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 3ML Syringe Luer Lock with needle 20GX1 Recalled by Fresenius Medical Care...

The Issue: There is a potential for blood backfill leakage and foreign material.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 8, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 10ML SYRINGE LUER LOCK W/NEEDLE Recalled by Fresenius Medical Care Holdings,...

The Issue: There is a potential for blood backfill leakage and foreign material.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 8, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 10ML SYRINGE LUER LOCK W/OUT NEEDLE Recalled by Fresenius Medical Care...

The Issue: There is a potential for blood backfill leakage and foreign material.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 8, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Iron_2 (IRON_2) Reagents Recalled by Siemens Healthcare...

The Issue: There is a potential for a positive bias on Quality Control (QC) and patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2023· GE Medical Systems Information Technologies Inc

Recalled Item: Prucka 3 Amplifiers Recalled by GE Medical Systems Information Technologies...

The Issue: A diode on the power supply of the Prucka 3 Amplifier used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2023· Oculus Optikgeraete GMBH

Recalled Item: Oculus Pentacam AXL Recalled by Oculus Optikgeraete GMBH Due to Their is a...

The Issue: Their is a potential that optical devices with insufficient anti- coating...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2023· Oculus Optikgeraete GMBH

Recalled Item: Oculus Myopia Master Recalled by Oculus Optikgeraete GMBH Due to Their is a...

The Issue: Their is a potential that optical devices with insufficient anti- coating...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2023· Oculus Optikgeraete GMBH

Recalled Item: Oculus Pentacam AXL Wave Recalled by Oculus Optikgeraete GMBH Due to Their...

The Issue: Their is a potential that optical devices with insufficient anti- coating...

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

Class II — Potential Health HazardOngoing
DrugAugust 7, 2023· Advanced Accelerator Applications USA, Inc.

Recalled Item: PLUVICTO 1 Recalled by Advanced Accelerator Applications USA, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: vials were labeled with...

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

Class III — Low RiskOngoing
Refund