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 1566115680 of 55,602 recalls

Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Wright Medical Technology Inc

Recalled Item: INBONE Total Ankle System Recalled by Wright Medical Technology Inc Due to...

The Issue: The package contents and package labeling do not match.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· Wright Medical Technology Inc

Recalled Item: INBONE Total Ankle System Recalled by Wright Medical Technology Inc Due to...

The Issue: The package contents and package labeling do not match.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· Medtronic Neuromodulation

Recalled Item: Medtronic Wireless Recharger Model WR9200 included in the RS6200 Recharger...

The Issue: The wireless rechargers (WR; WR9200 and WR9220; included in the Recharger...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· Medtronic Neuromodulation

Recalled Item: Medtronic Wireless Recharger Model WR9220 included in the RS5200 Recharger...

The Issue: The wireless rechargers (WR; WR9200 and WR9220; included in the Recharger...

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

Class II — Potential Health HazardOngoing
DrugNovember 3, 2021· Ascend Laboratories LLC

Recalled Item: Cefixime Capsules 400 mg Recalled by Ascend Laboratories LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 3, 2021· Haag-Streit USA Inc

Recalled Item: OCT-Camera 211 01 A3 Recalled by Haag-Streit USA Inc Due to Malfunction of...

The Issue: Malfunction of the automatic laser beam shut-off, the OCT unit might not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2021· Haag-Streit USA Inc

Recalled Item: OCT-Camera 211 01 A1 Recalled by Haag-Streit USA Inc Due to Malfunction of...

The Issue: Malfunction of the automatic laser beam shut-off, the OCT unit might not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2021· Leica Microsystems, Inc.

Recalled Item: Leica Microsystems M220 F12 Microscope Systems Recalled by Leica...

The Issue: In May 2021, Leica Microsystems received one (1) complaint pertaining to the...

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

Class II — Potential Health HazardOngoing
FoodNovember 2, 2021· Alsum Farms & Produce, Inc.

Recalled Item: Alsum Farms & Produce Whole Red onions packaged in 2lb. (907g) bags Recalled...

The Issue: Onions are being recalled by Keeler Family Farms due to potential Salmonella...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 2, 2021· Alsum Farms & Produce, Inc.

Recalled Item: Alsum Farms & Produce Whole White Onions Recalled by Alsum Farms & Produce,...

The Issue: Onions are being recalled by Keeler Family Farms due to potential Salmonella...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 2, 2021· Murray International Trading Co., Inc.

Recalled Item: "Herbal Doctor" brand Angelicae Sinensis Recalled by Murray International...

The Issue: Product contains elevated levels of lead and cadmium

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

Class II — Potential Health HazardOngoing
Refund