State

Georgia product recalls

20,364 recalls have nationwide distribution and so reach Georgia. 0 additional recalls listed Georgia specifically in their distribution scope.

About recalls in Georgia

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 Georgia 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 20364

HighFDA (Devices)·Z-0046-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Kit recalled for incorrect expiration date labeling
Hobbs Medical recalls the Freeman Pancreatic Flexi-Stent Kit due to incorrect expiration dates on product labels that extend shelf life. Affected devices were distributed to the US and international markets from March 2018 through September 2020.
Product
Freeman Pancreatic Flexi-Stent Kit (containing 6352) Catalog Number: 6321
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-0070-2023·2022-10-19
Hobbs Medical Polypectomy Snare Incorrect Expiration Date Label Recall
Hobbs Medical polypectomy snares have incorrect expiration dates on labels that extend the device shelf life beyond safe limits. Affected products distributed from March 2018 to September 2020 may be used past their intended expiration.
Product
Hobbs Medical Polypectomy Snare Catalog Number: 4575-OLY
Category
Medical Device
Distribution
Distributed nationwide
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-0052-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Kit Recalled for Mislabeled Expiration Dates
Hobbs Medical recalls Freeman Pancreatic Flexi-Stent kits with incorrect expiration dates on the label, which extends the stated shelf life and could allow use of expired devices.
Product
Freeman Pancreatic Flexi-Stent Kit (containing 6566) Catalog Number: 6518
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0067-2023·2022-10-19
Hobbs Medical Polypectomy Snare with Incorrect Expiration Date Label
Hobbs Medical is recalling Polypectomy Snares (Catalog 7202) with incorrect expiration dates on labels, which could allow use of expired devices. Units were distributed in the US and several other countries from March 2018 to September 2020.
Product
Hobbs Medical Polypectomy Snare Catalog Number: 7202
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0060-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Recall Due to Incorrect Expiration Date
Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices due to incorrect expiration dates on product labels. The incorrect dates extend the shelf life, potentially allowing use beyond the actual safe expiration.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6562
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0036-2023·2022-10-19
Hobbs Retrieval Forceps Recalled for Incorrect Expiration Dates
Hobbs Medical is recalling Retrieval Forceps with incorrect expiration dates on device labels. Affected devices distributed between March 2018 and September 2020 may be used past their actual expiration.
Product
Hobbs Retrieval Forceps Catalog Number: 5018
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-0024-2023·2022-10-19
Hobbs Posi-Stop Injection Needles Recalled for Incorrect Expiration Date Labeling
Hobbs Medical, Inc. is recalling Posi-Stop Injection Needles with lot numbers ending in 'R' due to incorrect expiration dates on device labels. The mislabeling extends the apparent shelf life, potentially allowing use of expired sterile devices.
Product
Hobbs Posi-Stop Injection Needle Catalog Number: 4720
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0016-2023·2022-10-19
Hobbs Medical Polypectomy Snare Recalled for Incorrect Expiration Date
Hobbs Medical is recalling Polypectomy Snare devices (Catalog Number 4564) due to incorrect expiration dates on labels that extend the stated shelf life. The 35 affected units, distributed in the US and select countries, may be used beyond their actual safe shelf life.
Product
Hobbs Medical Polypectomy Snare Catalog Number: 4564
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0055-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Recalled for Incorrect Expiration Date
Hobbs Medical recalled Freeman Pancreatic Flexi-Stents due to incorrect expiration dates on device labels. The mislabeled dates extend shelf life, potentially allowing use of expired devices.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6533
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
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-0083-2023·2022-10-19
Prismaflex HF medical device sets recalled for instructional mistranslation
Baxter Healthcare recalls Prismaflex HF Set devices due to a mistranslation in Estonian language instructions. The mistranslation contains contradictory information about patient body weight restrictions.
Product
Prismaflex HF Set: HF1000 (product code 107140), HF1400 (product code 107142). For use in providing continuous fluid management and renal replacement therapies.
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-0014-2023·2022-10-19
Hobbs Medical Cytology Brush Recalled for Incorrect Expiration Date Labeling
Hobbs Medical is recalling Cytology Brush Catalog Number 4206 due to incorrect expiration dates on product labels that extend the intended shelf life. Approximately 300 units were distributed nationwide and internationally between March 2018 and September 2020.
Product
Hobbs Medical Cytology Brush Catalog Number: 4206
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0021-2023·2022-10-19
Hobbs Posi-Stop Injection Needle recalled for incorrect expiration dates
Hobbs Medical is recalling Hobbs Posi-Stop Injection Needles due to incorrect expiration dates on device labels that extend the shelf life. Affected devices have lot numbers ending in 'R' distributed from 2018–2020.
Product
Hobbs Posi-Stop Injection Needle Catalog Number: 4704
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-0038-2023·2022-10-19
Hobbs Biliary Pigtail Stent Kits recalled due to incorrect expiration date
Hobbs Medical is recalling Biliary Pigtail Stent Kits with incorrect expiration dates on labels. The incorrect dates extend the product shelf life, potentially allowing devices to be used past their actual expiration.
Product
Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number:6004
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0011-2023·2022-10-19
Hobbs Medical Spray Catheter Recalled for Incorrect Expiration Date on Label
Hobbs Medical Spray Catheter devices sold between March 2018 and September 2020 have incorrect expiration dates on their labels. The error may extend the device's shelf life beyond its actual expiration.
Product
Hobbs Medical Spray Catheter: The Mistifier: 2.6mm 165cm Disposable For endoscopy procedures Ref: 2191
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0063-2023·2022-10-19
Pancreatic stent recall due to incorrect expiration date on device labels
Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices distributed between March 2018 and September 2020 due to incorrect expiration dates on product labels. The mislabeled devices display extended shelf-life information that does not reflect actual product safety.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6568
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0080-2023·2022-10-19
Clip COVID Rapid Antigen Test Kit Recalled for Unapproved Shelf-Life Extension
LUMINOSTICS recalled Clip COVID test kits because the manufacturer extended shelf life and expiration dates without FDA approval. The extended expiration dates lack FDA validation.
Product
Clip COVID Rapid Antigen Test Kit (25-pack), Catalog Number: MDL002
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-0048-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Kit recalled for mislabeled expiration dates
Hobbs Medical is recalling the Freeman Pancreatic Flexi-Stent Kit because the device label displays an incorrect expiration date that extends the shelf life. U.S. distribution of affected devices occurred between March 25, 2018 and September 28, 2020.
Product
Freeman Pancreatic Flexi-Stent Kit Catalog Number: 6352
Category
Medical Device
Distribution
Distributed nationwide