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. 2,067 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,067 in last 12 months

Showing 1494114960 of 55,602 recalls

FoodJanuary 10, 2022· Brownie Points LLC

Recalled Item: Brownie Points Schmurtle 2oz Packaged in food grade cellophane only Recalled...

The Issue: Contains Statement on Label does not include all allergens - Peanuts

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 10, 2022· Shimadzu Medical Systems

Recalled Item: MODEL: X-RAY TV SYSSTEM SONIALVISION safire17 Recalled by Shimadzu Medical...

The Issue: It was found that the irradiated x-ray may exceed the xray radiation dose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2022· Shimadzu Medical Systems

Recalled Item: MODEL: X-RAY TV SYSTEM SONIALVISION G4 Recalled by Shimadzu Medical Systems...

The Issue: It was found that the irradiated x-ray may exceed the xray radiation dose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2022· Shimadzu Medical Systems

Recalled Item: MODEL: X-RAY R/F SYSTEM FLUOROspeed X1 Recalled by Shimadzu Medical Systems...

The Issue: It was found that the irradiated x-ray may exceed the xray radiation dose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2022· BASE 10 GENETICS INC

Recalled Item: RNAstill Molecular Transport Medium Vial Recalled by BASE 10 GENETICS INC...

The Issue: The product does not have 510(k) clearance.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2022· Compass Health Brands (Corporate Office)

Recalled Item: Voyager Rollator-intended as a mechanical walker Model Number: RLEU10xx...

The Issue: Wheel spoke may crack causing the wheel to separate from the axle may result...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2022· Acon Biotech (Hangzhou) Co., Ltd.

Recalled Item: Flowflex SARS-CoV-2 Antigen Rapid Test (Self-Testing) Recalled by Acon...

The Issue: Non-EUA authorized, CE marked, SARS-CoV-2 antigen rapid test kits are being...

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

Class II — Potential Health HazardOngoing
DrugJanuary 7, 2022· Teva Pharmaceuticals USA

Recalled Item: Mimvey (estradiol and norethindrone acetate tablets USP) 1 mg/0.5 mg...

The Issue: Mislabeling

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

Class III — Low RiskOngoing
Refund
DrugJanuary 7, 2022· Teva Pharmaceuticals USA

Recalled Item: Mimvey (estradiol and norethindrone acetate tablets USP) Recalled by Teva...

The Issue: Mislabeling

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

Class III — Low RiskOngoing
Refund
DrugJanuary 7, 2022· VistaPharm, Inc.

Recalled Item: Clobazam Oral Suspension 2.5 mg/mL Recalled by VistaPharm, Inc. Due to...

The Issue: Failed Stability Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 7, 2022· Orthosoft, Inc. dba Zimmer CAS

Recalled Item: NavitrackER Kit A: Knee Recalled by Orthosoft, Inc. dba Zimmer CAS Due to...

The Issue: The product was released for distribution without passing sterilization...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2022· Biomet, Inc.

Recalled Item: Comprehensive Shoulder System Primary Shoulder Stem Recalled by Biomet, Inc....

The Issue: The products in scope underwent an incorrect rework operation for the porous...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2022· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System Recalled by Biomet, Inc. Due to The...

The Issue: The products in scope underwent an incorrect rework operation for the porous...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2022· Biomet, Inc.

Recalled Item: Comprehensive Shoulder System Mini Humeral Stem Recalled by Biomet, Inc. Due...

The Issue: The products in scope underwent an incorrect rework operation for the porous...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2022· Biomet, Inc.

Recalled Item: Comprehensive Shoulder System Mini Humeral Stem Recalled by Biomet, Inc. Due...

The Issue: The products in scope underwent an incorrect rework operation for the porous...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2022· Biomet, Inc.

Recalled Item: Comprehensive Shoulder System Mini Humeral Stem Recalled by Biomet, Inc. Due...

The Issue: The products in scope underwent an incorrect rework operation for the porous...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2022· Biomet, Inc.

Recalled Item: Comprehensive Shoulder System Primary Shoulder Stem Recalled by Biomet, Inc....

The Issue: The products in scope underwent an incorrect rework operation for the porous...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2022· Biomet, Inc.

Recalled Item: Comprehensive Shoulder System Mini Humeral Stem Recalled by Biomet, Inc. Due...

The Issue: The products in scope underwent an incorrect rework operation for the porous...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2022· Biomet, Inc.

Recalled Item: Comprehensive Shoulder System Primary Shoulder Stem Recalled by Biomet, Inc....

The Issue: The products in scope underwent an incorrect rework operation for the porous...

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

Class II — Potential Health HazardOngoing
FoodJanuary 6, 2022· Dole Fresh Vegetables Inc

Recalled Item: Marketside 12oz Classic Salad SKU: 3107 Recalled by Dole Fresh Vegetables...

The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...

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

Class I — Serious Health HazardOngoing
Refund