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. 1,836 recalls have been distributed to South Carolina in the last 12 months.
Showing 28981–29000 of 51,854 recalls
Recalled Item: BEQ-TOP 41201 ECC 3/8 PUMP PAC Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 24500 ADULT ECC Recalled by Datascope Corporation Due to The Better...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-T 9410 Lurie Chldns Small 1/4 Recalled by Datascope Corporation Due to...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 25500 ECC 3/8 w/QiD Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 24202 ADULT ECC Recalled by Datascope Corporation Due to The Better...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 40700 HUNTINGTON Recalled by Datascope Corporation Due to The Better...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 8504 1/4X1/4 PACK W/QP Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Small Patient ECC Pack BEQ-TOP 22301 Recalled by Datascope Corporation Due...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 50900 Custom ECC Pack-Neonatal 1/4 Recalled by Datascope Corporation...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 50903 Custom ECC Pack-Pedriatric Recalled by Datascope Corporation...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 33500 3/8" ECC PACK Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-T 25501 3/8" Better Bladder Pack Recalled by Datascope Corporation Due...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR Recalled by Johnson &...
The Issue: Some contact lenses were associated with complaints of a foreign matter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUVUE OASYS Brand Contact Lenses with HYDRACLEAR PLUS Recalled by Johnson &...
The Issue: Some contact lenses were associated with complaints of a foreign matter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses Recalled by Johnson...
The Issue: Some contact lenses were associated with complaints of a foreign matter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mallinckrodt Institute Percutaneous Gastrostomy Set Product Usage: Intended...
The Issue: Cook has identified that the affected lots may contain wire guides that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Gastrojejunostomy Set Product Usage: Intended for the...
The Issue: Cook has identified that the affected lots may contain wire guides that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wills-Oglesby Percutaneous Gastrostomy Set Product Usage: Intended for the...
The Issue: Cook has identified that the affected lots may contain wire guides that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex(R) Percuvance(TM) Percutaneous Surgical System Recalled by Teleflex...
The Issue: Teleflex is recalling these products because the jaws of the tool tip may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methylphenidate Hydrochloride Tablets USP Recalled by Teva Pharmaceuticals...
The Issue: Failed Dissolution Specifications: Low out of specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.