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. 925 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 52521–52540 of 55,602 recalls
Recalled Item: BREG Cold Therapy Combination Units containing Sterile Polar Pads. 02356 Rev...
The Issue: The recall was initiated because Breg has determined that some Sterile Polar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Senographe Essential System. The Senographe 2000D system...
The Issue: GE Healthcare has recently become aware of a potential issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeStyles ZERO 10 uber-thin lubricated latex condoms. Mfd. for Ansell...
The Issue: Out of an abundance of caution, Ansell is implementing a voluntary recall of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BREG Sterile Polar Pads Recalled by Breg Inc Due to The recall was initiated...
The Issue: The recall was initiated because Breg has determined that some Sterile Polar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atricure Inc. Recalled by Atricure Inc Due to Products from lot no. 41865...
The Issue: Products from lot no. 41865 may have been sent out with Incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare SureSigns VS2+ Model 863278 SureSigns VS2+ NBP and...
The Issue: VS2+ screen may lock up and stop monitoring during patient use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Titanium Midface Distractor Recalled by Synthes USA HQ, Inc. Due to...
The Issue: There is the potential for the anterior footplates to not fit onto the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Multi-Vector Distractor Body Recalled by Synthes USA HQ, Inc. Due to...
The Issue: It was discovered that the sheer pin on the Multi-Vector Distractor may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Dens Instrument Set (Dens Graphic Case) Recalled by Synthes USA HQ,...
The Issue: The Dens Instrument Set has been designed to facilitate the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx90 GUIDING CATH ST Product Code: GST60900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx100 GUIDING CATH MP Product Code: GMD61000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx100 GUIDING CATH ST Product Code: GST61000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx100 GUIDING CATH S2 Product Code: GSM61000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 5Fx100 GUIDING CATH HH Product Code: GMC51000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Oracle Spacer System Slap Hammer Recalled by Synthes USA HQ, Inc....
The Issue: This recall is being initiated in response to complaints received where it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx100 GUIDING CATH MC Product Code: GCB61000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx100 GUIDING CATH MPD Product Code: GMD60900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 5Fx90 GUIDING CATH ST Product Code: GST50900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx90 GUIDING CATH MPC Product Code: GMC60900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of packaging integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 14 x 40 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.