State
73,809 recalls have nationwide distribution and so reach Georgia. 9,635 additional recalls listed Georgia specifically in their distribution scope.
Of the 9,635 recalls naming Georgia we have scored against our rubric, 1,471 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,567 (27%) are Severe.
Which agencies issued them
These figures cover only the 9,635 recalls whose distribution notice names Georgia specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ethicon, Inc. is recalling PDS Plus Antibacterial Sutures because three lots were labeled with a five-year expiry date instead of the correct two-year date.
ICU Medical is recalling 11,500 smallbore extension sets manufactured with incorrect spin collars. The affected units were distributed in the US, Canada, and Japan.
Teleflex Medical Europe Ltd is recalling Simplastic Suprapubic Puncture Instruments because the packaging lacks a required warning that the products contain natural rubber latex.
United Pacific Co Ltd is recalling Zhong Hua Jiu (menthol 1%) Patches because they were produced with substandard GMP manufacturing processes.
ICU Medical is recalling 2,950 sterile 7-inch smallbore infusion sets because they were manufactured with an incorrect spin collar. The affected lots were distributed in the US, Canada, and Japan.
Ethicon is recalling PDS Plus Antibacterial Sutures because three lots were labeled with an incorrect five-year expiry date instead of the correct two-year date.
InvaGen Pharmaceuticals is recalling Decitabine for Injection because the product failed water content and impurity specifications.
Ethicon, Inc. is recalling specific lots of PDS Plus Antibacterial Sutures because they were labeled with an incorrect expiry date of five years instead of two.
ICU Medical is recalling 100 pouches of 5-inch Smallbore Extension Sets because they were manufactured with an incorrect spin collar.
Teleflex Medical Europe Ltd is recalling 6,340 rectal catheters because the packaging lacks a required warning that the product contains natural rubber latex.
Nidek Inc. is recalling 63 ARK-1s Auto Ref/Keratometers because there may be a difference between subjective and objective dioptric measurements.
Pepsi Cola Bottling Company is recalling Diet Pepsi 6-packs because the outer packaging incorrectly states the product is 'Now Aspartame Free' when it actually contains aspartame.
Aesculap Implant Systems LLC is recalling Doyen-Collin Mouth Gags because plastic sleeves may stick together, rendering the instruments unusable.
Bestco, Inc. is recalling Signature Care Calcium Chews because the packaging declares 25 mcg of Vitamin D, but the product actually contains 12.5 mcg.
The Magstim Company Limited is recalling 43 Magstim Rapid Therapy Systems because user manuals were not supplied with the devices.
Aesculap Implant Systems LLC is recalling Strauss Penis Clamps because plastic sleeves may stick together, rendering the instruments unusable.
KZRV is recalling 2018-2019 recreational trailers because the awning may deploy while moving, increasing the risk of a crash.
Harmony Juvenile Products is recalling Big Boost Deluxe booster seats because the seat belt may apply excessive force to a child's chest in a crash.
Lamborghini is recalling 11 2017 Centenario vehicles because an incorrect weight limit on the certification label may allow the vehicle to be overloaded.
KZRV is recalling 2019 Connect recreational trailers because an incorrect circuit breaker may increase the risk of a fire. Dealers will replace the part free of charge.
Schneider Electric is recalling Square D safety switches because power may remain on when the handle is in the OFF position, posing an electrical shock hazard.
Jo-Ann Stores is recalling battery-operated LED light sets because the glass jars can break during normal use, posing a laceration hazard.
Gulf Stream is recalling 2016-2018 Conquest and B Touring Cruiser motorhomes because they lack required intermediate side marker lights, increasing crash risk.
Ducati is recalling 2018 Panigale V4 motorcycles because fuel may leak from the gas tank valve plug, increasing the risk of fire.
Ducati is recalling 2018 Panigale V4 motorcycles because fuel may spray out of the tank when the cap is opened, increasing fire risk.