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. 2,460 recalls have been distributed to Mississippi in the last 12 months.
Showing 25601–25620 of 49,744 recalls
Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Digital PET/CT System Recalled by Philips Medical Systems...
The Issue: The block used to connect the patient pallet to the couch may be assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmniSure ROM Test under the following labels: 1) Catalog Number Recalled by...
The Issue: Potential for control line not appearing on the test strip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Recalled...
The Issue: Natus Neuro has discovered a possible manufacturing defect in the ErgoJust...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNI Hip System Recalled by OMNIlife science Inc. Due to The Internal...
The Issue: The Internal packaging, the pouch and patient labels are improperly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7K capsules packaged in single packs sold in 24-count boxes Recalled by...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found products to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: POSEIDON Xtreme PLATINUM 4500 Recalled by Shoreside Enterprises Inc. Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found products to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: My Way (Levonorgestrel) Tablets TWO PACK Recalled by Lupin Pharmaceuticals...
The Issue: Marketed Without an Approved NDA/ANDA: 2-pack configuration did not receive...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: My Way (levonorgestrel) Tablets TWO PACK Recalled by Lupin Pharmaceuticals...
The Issue: Marketed Without an Approved NDA/ANDA: 2-pack configuration did not receive...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Peripherally Inserted Midline Catheter Kit with Placement Wire Recalled by...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPS TipTracker Stylet Accessory Recalled by Arrow International Inc Due to...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPS Rhythm ECG Accessory Pack Recalled by Arrow International Inc Due to...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPS Rhythm ECG Accessory Pack with Johans Adapter Recalled by Arrow...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.