DC recalls
3294 federal recalls on file affecting DC - 218 DC-specific plus 3076 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2025-12-31FDA-DeviceCookClass IINationwideCheck Cook Ring Transjugular Access Sets for defects
Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification. Impacted products may have been cut to the incorrect length, not correctly trimmed, and not inspected properly.
- 2025-12-31FDA-DeviceCookClass IINationwideCheck Flexor introducer lot numbers immediately
Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification. Impacted products may have been cut to the incorrect length, not correctly trimmed, and not inspected properly.
- 2025-12-31FDA-DeviceDiasolClass IINationwideStop using Diasol dialysis concentrate
Safety and efficacy of dialysis acid concentrate cannot be assured
- 2025-12-31FDA-DeviceDiasolClass IINationwideBrand Name: Diasol Product Name: 100325-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0CA, 1.0MG, 208.2 liters
Safety and efficacy of dialysis acid concentrate cannot be assured
- 2025-12-31FDA-DeviceDiasolClass IINationwideStop using Diasol dialysis concentrate
Safety and efficacy of dialysis acid concentrate cannot be assured
- 2025-12-31FDA-DeviceDiasolClass IINationwideStop using Diasol dialysis concentrate
Safety and efficacy of dialysis acid concentrate cannot be assured
- 2025-12-31FDA-DeviceDiasolClass IINationwideStop using Diasol dialysis concentrate
Safety and efficacy of dialysis acid concentrate cannot be assured
- 2025-12-31FDA-DeviceDiasolClass IINationwideStop using Diasol dialysis concentrate
Safety and efficacy of dialysis acid concentrate cannot be assured
- 2025-12-31FDA-DeviceMicrobiologicsClass IINationwideCheck Microbiologics LYFO DISK Campylobacter jejuni lots
Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428.
- 2025-12-31FDA-DeviceMicrobiologicsClass IINationwideStop using Microbiologics KWIK-STIK cultures
Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428.
- 2025-12-31FDA-DeviceMicrobiologicsClass IINationwideStop using Microbiologics KWIK-STIK test kits
Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428.
- 2025-12-31FDA-DeviceZimmer BiometClass IINationwideContact your surgeon about Zimmer Affixus nail
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
- 2025-12-31FDA-DeviceZimmer BiometClass IINationwideContact your surgeon about Zimmer Affixus femoral nail
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
- 2025-12-31FDA-DeviceZimmer BiometClass IINationwideContact your surgeon about Zimmer femoral nail
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
- 2025-12-31FDA-DeviceZimmer BiometClass IINationwideContact your surgeon about Zimmer Affixus nail
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
- 2025-12-31FDA-DeviceZimmer BiometClass IINationwideContact your surgeon about Zimmer Affixus nail
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
- 2025-12-31FDA-DeviceZimmer BiometClass IINationwideContact your surgeon about Zimmer Affixus nail
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
- 2025-12-31FDA-DeviceZimmer BiometClass IINationwideContact your surgeon about Zimmer Affixus nail
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
- 2025-12-31FDA-DeviceZimmer BiometClass IINationwideContact your surgeon about Zimmer Affixus femoral nail
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
- 2025-12-31FDA-DeviceZimmer BiometClass IINationwideCheck if your femoral nail is affected
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
- 2025-12-31FDA-DeviceZimmer BiometClass IINationwideContact your surgeon about Zimmer Affixus nail
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
- 2025-12-31FDA-DeviceZimmer BiometClass IINationwideContact your surgeon about Zimmer femoral nail implant
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
- 2025-12-31FDA-DeviceZimmer BiometClass IINationwideContact your surgeon about Zimmer Affixus femoral nail
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
- 2025-12-31FDA-DeviceZimmer BiometClass IINationwideContact your surgeon about Zimmer Affixus nail
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
- 2025-12-31FDA-DeviceZimmer BiometClass IINationwideContact your surgeon about Zimmer Affixus femoral nail
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
- 2025-12-31FDA-DeviceZimmer BiometClass IINationwideCheck if you received Zimmer femoral nail implant
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
- 2025-12-31FDA-DeviceZimmer BiometClass IINationwideContact your surgeon about Zimmer femoral nail
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
- 2025-12-31FDA-DeviceZimmer BiometClass IINationwideContact your surgeon about Zimmer Affixus femoral nail
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
- 2025-12-31FDA-DeviceICU MedicalClass IINationwideStop using LifeShield Infusion Safety Software v2.2
Software issue only allows Concentration Limits to be defined to one digit of precision past the decimal point (0.1) instead of three digits (0.001). If the user is unable to use Concentration Limits as intended, they may need to change the limits to something other than what is recommended by the drug manufacturer, which may result in over- or under-delivery.
- 2025-12-31FDA-DeviceICU MedicalClass IINationwideCheck ICU Medical LifeShield Drug Library settings
For certain customers, the Change Summary review option ceases to operate as expected for any migrated library after the migration has been completed. Users must use alternate methods to review changes. Failure to do so may lead in over delivery, under delivery, or delay in setup on the infusion pump.
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