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. 2,906 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,906 in last 12 months

Showing 19611980 of 55,602 recalls

Medical DeviceJuly 22, 2025· Trinity Biotech USA

Recalled Item: Bartels ELISA Legionella Urinary Antigen. Model Number: B1029-440. In Vitro...

The Issue: Potential for Bartels ELISA Legionella Urinary Antigen kit B1029-440 lot 065...

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

Class II — Potential Health HazardOngoing
FoodJuly 21, 2025· Middlefield Original Cheese Cooperative

Recalled Item: 1) Middlefield Original Cheese Co-op 100% Grass-Fed Pepper Jack Cheese...

The Issue: Potential contamination with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 21, 2025· Middlefield Original Cheese Cooperative

Recalled Item: 1) Middlefield Original Cheese Co-op Monterey Jack Cheese Recalled by...

The Issue: Potential contamination with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 21, 2025· Middlefield Original Cheese Cooperative

Recalled Item: Paneer Cheese Recalled by Middlefield Original Cheese Cooperative Due to...

The Issue: Potential contamination with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 21, 2025· Middlefield Original Cheese Cooperative

Recalled Item: Middlefield Original Cheese Co-op Horseradish Flavored Cheese Recalled by...

The Issue: Potential contamination with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 21, 2025· Ascend Laboratories, LLC

Recalled Item: Amlodipine and Olmesartan Medoxomil Tablets Recalled by Ascend Laboratories,...

The Issue: Failed Dissolution Specifications: low dissolution results

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 21, 2025· Merck & Co. Inc

Recalled Item: Belsomra (suvorexant) tablets Recalled by Merck & Co. Inc Due to Failed...

The Issue: Failed Dissolution Specifications: potential for delayed dissolution of the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 21, 2025· B.Braun Medical S.A.S.

Recalled Item: Brand Name: CELSITE Product Name: CELSITE BABYPORT SET PUR 4 Recalled by...

The Issue: The potential for minor injury such as damage to the vessel and/or tearing...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2025· Tandem Diabetes Care, Inc.

Recalled Item: Battery Operated infusion pumps. t:slim X2 G5 Recalled by Tandem Diabetes...

The Issue: Insulin pumps manufactured with speakers from Revision A and B may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 21, 2025· Diagnostica Stago, Inc.

Recalled Item: STA-Liquid Anti-Xa 4. Model/Catalog Number: 00311US. The STA - Liquid...

The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2025· Diagnostica Stago, Inc.

Recalled Item: STA Satellite. Product Code: All . All software versions. The Recalled by...

The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2025· Diagnostica Stago, Inc.

Recalled Item: STA-Liquid Anti-Xa 8. Model/Catalog Number: 00322US. The STA - Liquid...

The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2025· Diagnostica Stago, Inc.

Recalled Item: STA - Fibrinogen 5. Model/Catalog Number: 00674. The STA - Recalled by...

The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2025· Insightra Medical Inc

Recalled Item: Brand Name: Ultra IABP Catheter Kit Product Name: Ultra IABP Recalled by...

The Issue: Device contains indications for use and device compatibility claims that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2025· Encore Medical, LP

Recalled Item: Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID...

The Issue: Their is a potential that the reamer may kick or bind up during or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2025· Encore Medical, LP

Recalled Item: Brand Name: DJO SURGICAL Product Name: FA S Altivate Reverse Recalled by...

The Issue: Their is a potential that the reamer may kick or bind up during or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2025· Encore Medical, LP

Recalled Item: Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID...

The Issue: Their is a potential that the reamer may kick or bind up during or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2025· Encore Medical, LP

Recalled Item: Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID...

The Issue: Their is a potential that the reamer may kick or bind up during or...

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

Class II — Potential Health HazardOngoing
DrugJuly 17, 2025· DermaRite Industries, LLC

Recalled Item: PeriGiene Recalled by DermaRite Industries, LLC Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Drug Product: The products were found...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 17, 2025· DermaRite Industries, LLC

Recalled Item: DermaSarra Recalled by DermaRite Industries, LLC Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Drug Product: The products were found...

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

Class I — Serious Health HazardOngoing
Refund