Product Recalls in South Carolina
Product recalls affecting South Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to South Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,529 recalls have been distributed to South Carolina in the last 12 months.
Showing 27601–27620 of 28,688 recalls
Recalled Item: SpiraLok 6.5 w/Needles with Orthocord Product Number: 222970 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 5.0 w/Needles with violet and blue Orthocord Product Number:...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 5.0mm with Panacryl without needles Product Number: 222965 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 5.0mm with Ethibond and needles Product Number: 222960 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 5.0 w/Needles with Orthocord Product Number: 222968 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 6.5mm with Ethibond and needles Product Number: 222962 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 5.0mm with Ethibond without needles Product Number: 222964 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 6.5mm with Panacryl and needles Product Number: 222963 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 5.0 w/out Needles with Orthocord Product Number: 222969 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 5.0 w/out Needles with violet and blue Orthocord Product Recalled...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Recalled by Gynex Corporation Due to The wrong electrical connector...
The Issue: The wrong electrical connector pin was attached to the cord during assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 6.5mm with Ethibond without needles Product Number: 222966 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 6.5 w/Needles with violet and blue Orthocord Product Number:...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 5.0mm with Panacryl and needles Product Number: 222961 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray DPM5 Monitor Recalled by Mindray DS USA, Inc. d.b.a. Mindray North...
The Issue: Mindray has identified an issue with the DPM5 monitors where ST and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hip Components: INSERT MOBILE "COLLEGIA" TAILLE 58*28 Recalled by Wright...
The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATS 3000 Automatic Tourniquet System w/HOSES AND LOP SENSOR Intended...
The Issue: Zimmer is conducting a voluntary removal of some Zimmer A.T.S. 3000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Components: ROTULE "913" D=32 Recalled by Wright Medical Technology Inc...
The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extremity Components: PROTHESE A EXPANSION COMPLETE D=6 LG 12 MM Recalled by...
The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NCB¿ cancellous screw Recalled by Zimmer, Inc. Due to Zimmer Inc., is...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.