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. 2,635 recalls have been distributed to Mississippi in the last 12 months.
Showing 6241–6260 of 49,744 recalls
Recalled Item: Intera 1.5T Master/Nova Recalled by Philips North America Llc Due to Patient...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T CX Recalled by Philips North America Llc Due to Patient support...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE AFFIXIUM Cementless Fixed Bearing Knee with 3DP Technology Recalled...
The Issue: Product incorrectly labelled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OsmoPRO MAX Automated Osmometer- IVD Osmometer for Clinical Use. Uses...
The Issue: System error messages may delay the ability to test patient samples and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Identity Imprint PS Tibial Tray Size 4: Lot 540287 Recalled by Conformis,...
The Issue: Size 5 Tibial Tray from Lot 508287 was packaged in a Size 4 box from Lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS EDGE 300ML CANISTER WITH Solidifier- Indicated for patients who...
The Issue: Black particulate matter from the carbon filter component of the canisters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS EDGE 800ML CANISTER WITH Solidifier- Indicated for patients who...
The Issue: Black particulate matter from the carbon filter component of the canisters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ureteral dilator Recalled by Coloplast Manufacturing US, LLC Due to A...
The Issue: A possible sterility issue (e.g. a breach in sterile packaging) was detected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HDS Traction Boot II Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Galaxy System (specifically GAL-019 Recalled by Noah Medical Due to Due to a...
The Issue: Due to a misaligned calibration of the wired controller that may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SWAD BRAND CINNAMON POWDER in clear plastic 3.5 OZ bags Recalled by RAJA...
The Issue: Product tested positive for lead
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Great Value Honey Roasted Cashews Recalled by John B. Sanfilippo & Son Inc....
The Issue: undeclared milk and coconut
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tri-Lo-Sprintec (norgestimate and ethinyl estradiol) tablets USP - triphasic...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...
The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...
The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...
The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Supreme Tradition brand and Marcum brand ground cinnamon. Packaged in...
The Issue: Elevated lead levels in cinnamon
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Potassium Chloride for Injection Concentrate USP Recalled by B. Braun...
The Issue: Lack of assurance of sterility: pinholes, within the blue label characters...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CryoValve SG Cryopreserved Pulmonary Human Heart Valve Recalled by Artivion,...
The Issue: The blood cultures performed as part of the organ donation process were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STIK Rhizopus stolonifer (+) derived from ATCC 6227b Recalled by...
The Issue: The positive control material (Rhizopus stolonifer) within the KWIK-STIK...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.