Product Recalls in Missouri
Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,945 recalls have been distributed to Missouri in the last 12 months.
Showing 17421–17440 of 29,298 recalls
Recalled Item: smith&nephew TRIGEN INTERTAN 10S Recalled by Smith & Nephew, Inc. Due to A...
The Issue: A single lot of INTERTAN 10S 10 MM X 18 CM 130 D was manufactured with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL800 analyzer with FLEXQ module. Device intended for in vitro Recalled by...
The Issue: Due to misinterpretation of the barcode by the scanner, when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensicare Green Surgical Glove Recalled by Medline Industries Inc Due to...
The Issue: Possible open seal on top portion of the package. Could cause breach of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARVEST TERUMOBCT Recalled by Terumo BCT, Inc. Due to Certain lots of the...
The Issue: Certain lots of the Harvest Graft Delivery System GDP-10 Procedure Packs may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARVEST(R) TERUMOBCT Recalled by Terumo BCT, Inc. Due to The patient labels...
The Issue: The patient labels included in the BMAC system procedure packs, catalog...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARVEST(R) TERUMOBCT Recalled by Terumo BCT, Inc. Due to The patient labels...
The Issue: The patient labels included in the BMAC system procedure packs, catalog...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound Transducer Recalled by Hitachi Medical Systems America Inc Due to...
The Issue: The ultrasound probe may not have adequate protection against electrical...
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: BO-TOP 20705 SMALL PATIENT 1/4 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: BEQ-TOP 22701 Recalled by Datascope Corporation Due to The Better Bladder...
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: NICU ECC Pack BEQ-TOP 39202 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 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: 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: BO-TOP 13901 RAPID RESPONSE 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 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: 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: ECC Small - Respiratory BEQ-TOP 5210 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: 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.