Product Recalls in Mississippi
Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,614 recalls have been distributed to Mississippi in the last 12 months.
Showing 12381–12400 of 28,172 recalls
Recalled Item: (1) Arrow¿ STIM CPNB TUOHY NDL: 18G x 14CM (5-1/2") Recalled by Arrow...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL CATHETERIZATION KIT CK-02220 Recalled by Arrow International...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Maximal Barrier Drape ASK-00002-1A Recalled by Arrow International Inc...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Pressure Injectable Two-Lumen PICC Kit 5 Fr. x 50 cm EU-05052-HPMSB...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL CATHETERIZATION KIT AM-05500 Recalled by Arrow International...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow SPINAL ANESTHESIA SET ASA-25090-S Recalled by Arrow International Inc...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL NEEDLE KIT SL-05500 Recalled by Arrow International Inc Due...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ EPIDURAL CATHETERIZATION KIT AK-05000 Recalled by Arrow International...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL NEEDLE COMPONENT AN-05505 Recalled by Arrow International Inc...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ARTIS pheno Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: The potential exists for system movement to be permanently blocked by an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or...
The Issue: Monitor/Defibrillator may not deliver a shock after the "Shock" button on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 MONITOR/DEFIBRILLATOR service kits Recalled by Physio-Control,...
The Issue: Monitor/Defibrillator may not deliver a shock after the "Shock" button on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAINLESS STEEL REPROCESSING TRAY Recalled by Intuitive Surgical, Inc. Due...
The Issue: Small but detectable holes in the sterilization wrap used with the firm's 8...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAINLESS STEEL REPROCESSING TRAY Recalled by Intuitive Surgical, Inc. Due...
The Issue: Small but detectable holes in the sterilization wrap used with the firm's 8...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Daytona Plus (with ISE/without ISE) Recalled by Randox Laboratories,...
The Issue: Software version UI2550642107 for the RX Daytona + instrument released to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost GCF Recalled by Philips Medical Systems Gmbh, DMC Due to When...
The Issue: When using the Table Up/Down button, the system may experience Error 80,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost PCF Recalled by Philips Medical Systems Gmbh, DMC Due to When...
The Issue: When using the Table Up/Down button, the system may experience Error 80,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation stand-alone software treatment planning system. Models 4.0...
The Issue: Three issues found: i) The Map ROI options in the ROI list in the Structure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Recalled by Zimmer...
The Issue: Potential issue associated with the instrument -end of the shaft could fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polysorb Braided Absorbable Suture 6/0 18" UNDYED P-10 Recalled by Covidien...
The Issue: There is a potential for packaging integrity issues impacting the humidity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.