State

South Carolina product recalls

20,371 recalls have nationwide distribution and so reach South Carolina. 0 additional recalls listed South Carolina specifically in their distribution scope.

About recalls in South Carolina

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect South Carolina consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

15351–15375 of 20371

HighFDA (Devices)·Z-0050-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Kits Recalled Due to Incorrect Expiration Dates
Freeman Pancreatic Flexi-Stent Kits are recalled due to device labels displaying incorrect expiration dates that extend shelf life. Affected units were distributed in the US and select countries from March 2018 to September 2020.
Product
Freeman Pancreatic Flexi-Stent Kits: Single Pigtail (containing 6544) Catalog Number: 6503
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0061-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Recall Due to Incorrect Expiration Dates
Hobbs Medical recalled Freeman Pancreatic Flexi-Stent devices due to incorrect expiration dates on labels that extend the shelf life, potentially allowing use beyond intended timeframe.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6566
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0065-2023·2022-10-19
Freeman Pancreatic Flexi-Stent label displays incorrect expiration date
Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices with incorrect expiration dates on their labels. The labeling error extends the shelf life beyond the intended timeframe.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6584
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0015-2023·2022-10-19
Hobbs Medical Polypectomy Snare recalled for incorrect expiration date on label
Hobbs Medical is recalling its Polypectomy Snare for an incorrect expiration date on the label that extends shelf life. Affected devices were distributed in the US and other countries from March 2018 to September 2020.
Product
Hobbs Medical Polypectomy Snare Catalog Number: 4563
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0039-2023·2022-10-19
Hobbs Biliary Pigtail Stent Kits recalled for incorrect expiration date
Hobbs Medical recalls biliary stent kits with incorrect expiration dates that extend shelf life. The kits were distributed from 2018 to 2020 in the US and select countries.
Product
Hobbs Biliary Pigtail Stent Kits (containing 6105) Catalog Number: 6023
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0022-2023·2022-10-19
Hobbs Posi-Stop Injection Needle Recall - Incorrect Expiration Date
Hobbs Medical is recalling Posi-Stop Injection Needles due to incorrect expiration dates on device labels that extend shelf life. Devices distributed between March 2018 and September 2020 could be used beyond their actual expiration.
Product
Hobbs Posi-Stop Injection Needle Catalog Number: 4712
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0034-2023·2022-10-19
Hobbs Medical Grasping Forceps Recalled for Incorrect Expiration Date Labeling
Hobbs Medical, Inc. is recalling Grasping Forceps due to incorrect expiration dates on device labels. Affected devices may be used beyond their safe shelf life if the mislabeled expiration dates are not corrected.
Product
Hobbs Medical Grasping Forceps Catalog Number:5004
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0059-2023·2022-10-19
Freeman Pancreatic Flexi-Stent labeled with incorrect expiration dates
Hobbs Medical is recalling Freeman Pancreatic Flexi-Stents with incorrect expiration dates on device labels that extend shelf life. Devices were distributed in the US and internationally from March 2018 to September 2020.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6548
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0045-2023·2022-10-19
Hobbs Biliary Pigtail Stent Kits Recalled Due to Incorrect Expiration Date Label
Hobbs Medical is recalling Biliary Pigtail Stent Kits distributed from March 2018 to September 2020 due to incorrect expiration date labels that extend the shelf life beyond the actual safe period.
Product
Hobbs Biliary Pigtail Stent Kits Catalog Number: 6108
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0047-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Kit Recall: Incorrect Expiration Date Label
Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent Kits with incorrect expiration dates on labels, potentially allowing devices to be used beyond their actual safe shelf life. Affected units were distributed from March 2018 to September 2020.
Product
Freeman Pancreatic Flexi-Stent Kit Catalog Number: 6351
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0035-2023·2022-10-19
Hobbs Medical Grasping Forceps Recalled for Incorrect Expiration Dates
Hobbs Medical Grasping Forceps (Catalog 5008) were distributed with incorrect expiration dates that extend shelf life beyond the device's actual safe use period. Affected units with lot numbers ending in 'R' were distributed from March 2018 to September 2020.
Product
Hobbs Medical Grasping Forceps Catalog Number: 5008
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0040-2023·2022-10-19
Hobbs Biliary Pigtail Stent Kits Recalled for Incorrect Expiration Date Labels
Hobbs Medical is recalling Biliary Pigtail Stent Kits for incorrect expiration dates on product labels that may extend shelf life. Affected kits were distributed nationwide and internationally between March 2018 and September 2020.
Product
Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6024
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0084-2023·2022-10-19
Prismaflex ST Renal Therapy Sets Recalled for Mistranslated Safety Instructions
Baxter Healthcare is recalling 1,068,560 Prismaflex ST renal replacement therapy sets nationwide. The recall is due to a mistranslation in the Estonian instructions that contains contradictory information about patient weight restrictions.
Product
Prismaflex ST Set: ST60 (product code 107643), ST100 (product code 107636), ST150 (product code 107640). For use in providing continuous fluid management and renal replacement therapies.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0019-2023·2022-10-19
Hobbs Scope Introducer Recalled for Incorrect Label Expiration Date
Hobbs Medical is recalling 140 units of its Hobbs Scope Introducer due to incorrect label expiration dates that extend the shelf life. Affected devices were distributed in the US and internationally from March 2018 to September 2020.
Product
Hobbs Scope Introducer Catalog Number: 4650
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0017-2023·2022-10-19
Hobbs Transbronchial Aspiration Needle Recalled for Incorrect Expiration Date
Hobbs Medical is recalling transbronchial aspiration needles with incorrect expiration dates on labels. The 18 affected units were distributed in the US, Canada, Austria, Belgium, Finland, and Norway from March 2018 to September 2020.
Product
Hobbs Transbronchial Aspiration Needle and Vacu-lok Aspirating Syringe Catalog Number: 4620
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0058-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Distributed with Incorrect Expiration Date
Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices due to incorrect expiration dates on the device labels. Affected units distributed in the US and internationally from March 2018 to September 2020 may have been used beyond their actual safe shelf life.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6544
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0013-2023·2022-10-19
Hobbs Medical Cytology Brush Recalled for Incorrect Expiration Dates
Hobbs Medical is recalling its Cytology Brush (catalog 4204) because device labels show incorrect expiration dates that extend the claimed shelf life. Affected devices were distributed in the US and several other countries from March 2018 to September 2020.
Product
Hobbs Medical Cytology Brush Catalog Number: 4204
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0010-2023·2022-10-19
Hobbs Medical Spray Catheter Recalled for Incorrect Expiration Date
Hobbs Medical is recalling Spray Catheter devices due to incorrectly labeled expiration dates that extend shelf life beyond the actual safe-use period. The recall affects 275 units distributed between March 2018 and September 2020.
Product
Hobbs Medical Spray Catheter: The Mistifier: 2.6mm 260cm Disposable For endoscopy procedures Ref: 2190
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0064-2023·2022-10-19
Freeman Pancreatic Flexi-Stent recalled for incorrect expiration date
Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices with incorrect expiration dates on labels that extend perceived shelf life beyond actual device longevity.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6582
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0033-2023·2022-10-19
Hobbs Helical Retrieval Basket Recalled for Incorrect Expiration Date
Hobbs Medical, Inc. is recalling Hobbs Helical Retrieval Baskets with lot numbers ending in R due to incorrect expiration dates on device labels. Affected units were distributed worldwide from March 2018 to September 2020.
Product
Hobbs Helical Retrieval Basket Catalog Number: 4832
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0068-2023·2022-10-19
Hobbs Medical Polypectomy Snare Recalled for Incorrect Expiration Dates
Hobbs Medical is recalling polypectomy snares with incorrect expiration dates on labels. Affected devices have lot numbers ending in R and were distributed from March 2018 to September 2020.
Product
Hobbs Medical Polypectomy Snare Catalog Number: 4563-OLY
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0028-2023·2022-10-19
Medical Device Retrieval Basket Recalled for Incorrect Expiration Date
Hobbs Medical is recalling Helical Retrieval Baskets with incorrect expiration dates on labels. The labeled shelf life extends beyond the actual safe duration for device use.
Product
Hobbs Helical Retrieval Basket Catalog Number: 4814
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0029-2023·2022-10-19
Hobbs Helical Retrieval Basket Recall: Incorrect Device Label Expiration Date
Hobbs Medical is recalling Helical Retrieval Baskets due to incorrect expiration dates on device labels. The mislabeling extends the shelf life, potentially allowing use of expired devices.
Product
Hobbs Helical Retrieval Basket Catalog Number: 4816
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0057-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Recall Due to Incorrect Expiration Date Label
Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices with incorrect expiration dates on labels. Affected units distributed in the US and internationally from 2018 to 2020 may have extended shelf lives beyond accuracy.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6535
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0085-2023·2022-10-19
Prismaflex HF20 Medical Device Recall Due to Mistranslated Instructions
Baxter Healthcare recalls the Prismaflex HF20 Set due to a mistranslation in device instructions that creates contradictory information about patient weight restrictions. The issue affects 29,764 devices distributed nationwide.
Product
Prismaflex HF20 Set (product code 109841). For use in providing continuous fluid management and renal replacement therapies.
Category
Medical Device
Distribution
Distributed nationwide