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. 968 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
968 in last 12 months

Showing 43261–43280 of 55,602 recalls

DrugMarch 10, 2015· the Compounder

Recalled Item: BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)...

The Issue: Recalled products were made using an active ingredient that was recalled by...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2015· the Compounder

Recalled Item: BIEST TD 80/20 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3))...

The Issue: Recalled products were made using an active ingredient that was recalled by...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: TUBING SET 7/8" X 6' WITH 1/4" x 24" TUBING Recalled by Microtek Medical Inc...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: FREEDOMAIRE(R) HELMET SYSTEM WITH BELT Recalled by Microtek Medical Inc Due...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: FREEDOMAIRE(R) HELMET WITH MOTOR MODULE Recalled by Microtek Medical Inc Due...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: Smoke Evacuation Tubing Set for Coherent CPG Handpiece Recalled by Microtek...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: FREEDOMAIRE(R) MOTOR MODULE Recalled by Microtek Medical Inc Due to This...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: TUBING 7/8' X 10' Recalled by Microtek Medical Inc Due to This recall is...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: LASER RESISTANT WAND - STERILE Recalled by Microtek Medical Inc Due to This...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm) Recalled by Microtek Medical Inc...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: LAPAROSCOPIC TUBING SET Recalled by Microtek Medical Inc Due to This recall...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Zimmer, Inc.

Recalled Item: Brand Name: Persona¿ Anterior Sizer with Locking Boom The Recalled by...

The Issue: Zimmer, Inc is voluntarily recalling 22 lots of Persona¿ Anterior Sizer with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· US Endoscopy Group Inc

Recalled Item: Talon Grasping Device Recalled by US Endoscopy Group Inc Due to A wire...

The Issue: A wire component on the distal grasping assembly of the device became detached..

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm) Recalled by Microtek Medical Inc...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: INTEGRAL WAND W/TUBING Recalled by Microtek Medical Inc Due to This recall...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: (S) TUBE SET 1/4" X 10' (0.64 cm X 304.8 cm) with 7/8" (2.22 cm) Adaptor...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: FREEDOMAIRE(R) HELMET SYSTEM WITH SUPER POWER PAK BATTERY Recalled by...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Nobel Biocare Usa Llc

Recalled Item: NobelReplace CC RP 4.3x10mm Recalled by Nobel Biocare Usa Llc Due to A...

The Issue: A material used in the packaging of the dental implants may impart a sticky...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to GE Healthcare has become...

The Issue: GE Healthcare has become aware of a potential safety issue involving MRI...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Nobel Biocare Usa Llc

Recalled Item: NobelReplace CC RP 4.3x8mm Recalled by Nobel Biocare Usa Llc Due to A...

The Issue: A material used in the packaging of the dental implants may impart a sticky...

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

Class II — Potential Health HazardOngoing