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. 1,716 recalls have been distributed to South Carolina in the last 12 months.
Showing 50081–50100 of 51,854 recalls
Recalled Item: florAlign Prebiotic Formula Recalled by Eco Health, Inc. Due to Potential...
The Issue: Eco Health is recalling florAlign Prebiotic Formula because it has the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1/2" Diced Yellow Onions Recalled by Gills Onions, LLC Due to Potential...
The Issue: Gills Onions is recalling diced and slivered onions because it may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1/4" Slivered Yellow Onions Recalled by Gills Onions, LLC Due to Potential...
The Issue: Gills Onions is recalling diced and slivered onions because it may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 3/16" Slivered Red Onions Recalled by Gills Onions, LLC Due to Potential...
The Issue: Gills Onions is recalling diced and slivered onions because it may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1/4" Diced Red Onions Recalled by Gills Onions, LLC Due to Potential...
The Issue: Gills Onions is recalling diced and slivered onions because it may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
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 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 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: 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: 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 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 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 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: SpiraLok 6.5 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: Screw Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co. Due to Fracture...
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: Philips Digital Diagnost-Mobile Detector Holder for Digital Diagnost (Single...
The Issue: The Wireless Portable Detector (WPD) is not fixed securely inside the Mobile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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 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.