Alabama recalls
4284 federal recalls on file affecting Alabama - 367 Alabama-specific plus 3917 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-07-01FDA-DeviceMedlineClass IINationwideMedline syringe kits recalled for unapproved design changes
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
- 2026-07-01FDA-DeviceMedlineClass IINationwideMedline surgical kits recalled for unapproved design changes
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
- 2026-07-01FDA-DeviceMedlineClass IINationwideMedline syringe kits recalled for unapproved design changes
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
- 2026-07-01FDA-DeviceMedlineClass IINationwideConvenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. BARIATRIC DYNJ905153J DYNJ905153K DYNJ905153L GYNE LAPAROTOMY PACK-LF DYNJ49593A LAPAROSCOPY DYNJ905157G DYNJ905157I DYNJ905157J LAPAROSCOPY PACK DYNJ56930B MAJOR PLUS PACK DYNJ905160J DYNJ905160K DYNJ905160M MINIMALLY INVASIVE PACK-LF DYNJ0843063K PERCUTANEOUS TRAY DYNJ80196 ROBOTIC PACK DYNJ908706 DYNJ908706B
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
- 2026-07-01FDA-DeviceMedlineClass IINationwideMedline convenience kits recalled for unapproved design changes
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
- 2026-07-01FDA-DeviceMedlineClass IINationwideMedline syringe kits recalled for unapproved design changes
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
- 2026-07-01FDA-DeviceBoston ScientificClass IINationwideBoston Scientific INTERA 3000 pump recalled for drug leakage risk
There is the potential for leakage along the drug pathway from the pump through the end of the catheter.
- 2026-07-01FDA-DevicePhilipsClass IINationwidePhilips Telemetry Monitor 5500 recalled for reset risk
Potential for device reset to default "NEW_DEVICE" state, which may lead to a to loss of device configuration and the equipment label, resulting in a failure to reconnect to the PIC iX central monitoring system.
- 2026-07-01FDA-DeviceZimmer BiometClass IINationwideZimmer Persona Revision augment recalled for packaging error
Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.
- 2026-07-01FDA-DeviceMedtronicClass IINationwideMedtronic Octopus 4 Tissue Stabilizer recalled for assembly error
During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister, and the long tube was attached to the top, contrary to the intended design.
- 2026-07-01FDA-DeviceMedtronicClass IINationwideMedtronic Octopus Evolution AS Tissue Stabilizer recalled for tubing assembly error
During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister, and the long tube was attached to the top, contrary to the intended design.
- 2026-07-01FDA-DeviceMedtronicClass IINationwideMedtronic Octopus Evolution Tissue Stabilizer recalled for assembly error
During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister, and the long tube was attached to the top, contrary to the intended design.
- 2026-07-01FDA-DeviceDexcomClass IINationwideDexcom G7 sensors recalled for infection and accuracy risks
Certain lots of Dexcom G7 sensors originally designated as scrap and intended for destruction were stolen during the destruction process. The sensors were later sold to pharmacies and distributors by Pharmsource, LLC. Lot 1725204004 were designated for destruction because the G7 sensors were not properly sterilized and have an increased risk of skin infection if used. Lot 1725069002 were designated for destruction due to an increased risk of having no sensor readings available or experiencing sensor inaccuracy that includes the potential for missed detection of a hyperglycemic event or incorrect treatment decisions that can result in patient injury, including medical intervention to prevent permanent injury or impairment. Additionally, due to the unknown storage and handling and storage conditions these sensors may have undergone during the distribution, these sensors may present additional risk.
- 2026-07-01FDA-DeviceSurgify MedicalClass IINationwideSurgify Halo burr recalled for breakage during spinal surgery
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- 2026-07-01FDA-DeviceSurgify MedicalClass IINationwideSurgify Halo burr recalled for breakage risk during spine surgery
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- 2026-07-01FDA-DeviceSurgify MedicalClass IINationwideSurgify Halo burr recalled for breakage risk
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- 2026-07-01FDA-DeviceSurgify MedicalClass IINationwideSurgify Halo burr recalled for breakage risk
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- 2026-07-01FDA-DeviceSurgify MedicalClass IINationwideSurgify Halo burr recalled for breakage risk in spine surgery
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- 2026-07-01FDA-DeviceSurgify MedicalClass IINationwideSurgify Halo surgical burr recalled for breakage risk
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- 2026-07-01FDA-DeviceSurgify MedicalClass IINationwideSurgify Halo burr recalled for breakage risk in spinal surgery
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- 2026-07-01FDA-DeviceSurgify MedicalClass IINationwideSurgify Halo burr recalled for breakage risk in spinal surgery
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- 2026-07-01FDA-DeviceSurgify MedicalClass IINationwideSurgify Halo burr recalled for breakage risk in spinal surgery
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- 2026-07-01FDA-DeviceSurgify MedicalClass IINationwideSurgify Halo burr recalled for breakage risk
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- 2026-07-01FDA-DeviceSurgify MedicalClass IINationwideSurgify Halo spinal burr recalled for breakage risk
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- 2026-07-01FDA-DeviceSurgify MedicalClass IINationwideSurgify Halo burr recalled for breakage risk in spinal surgery
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- 2026-07-01FDA-DeviceSurgify MedicalClass IINationwideSurgify Halo surgical burr recalled for breakage risk
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- 2026-07-01FDA-DeviceSurgify MedicalClass IINationwideSurgify Halo surgical burr recalled for breakage risk
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- 2026-07-01FDA-DeviceSurgify MedicalClass IINationwideSurgify Halo spinal burr recalled for breakage risk
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- 2026-07-01FDA-DeviceSurgify MedicalClass IINationwideSurgify Halo burr recalled for breakage risk in spinal surgery
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- 2026-07-01FDA-DeviceSurgify MedicalClass IINationwideSurgify Halo burr recalled for breakage risk
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
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